DEVICE RAC Exam 2025–2026 Accurate Real Exam
Questions and Verified Correct Answers JUST
RELEASED
A handling and storage system for medical devices must always include:
A. Procedures for rotation of stock
B. Separate rooms or cages for release and quarantine products
C. Procedures for receipt and transfer of product
D. Environmentally controlled areas for products with shelf life
C
Which of the following is exempt from GMP/QSR regulations?
A. Remanufacturers
B. Custom device manufacturers
C. Repackagers
D. Component manufacturers
D
Which division would have primary jurisdiction over a vascular graft with an antibiotic based on primary
mode of action?
A. CDER
B. CBER
C. CDRH
D. OCP
C
According to the Quality System Regulations, re-testing and re-evaluation of nonconforming devices
after rework activities must be documented in the:
A. Device history record
B. Device master record
C. Quality manual
D. Design history file
A
,Under the statutory violations, failure to meet 510(k) requirements for a device that is required to have
a 510(k) and is in commercial distribution is considered to be:
A. Adulteration.
B. Improper use
C. Misbranded
D. Fraudulent
C
A company's competitor is marketing a Class II suture which dissolves during the third week of use. The
company's current product has to be removed by a physician. However, a change in weaving
configuration gives this product the same dissolving time as the competitor's. When can the company's
new suture be marketed?
A. This requires a new 510(k) since significant change in product instructions might
affect efficacy.
B. After submission in a periodic report
C. After reporting clinical studies in an annual report
D. After submission of labeling change
A
A physician reports to a manufacturer that a patient was hospitalized with acute sepsis after treatment
with an approved device. This side effect is not listed in the package insert. This event must be reported
by the manufacturer to FDA no later than:
A. 5 calendar days
B. 15 calendar days
C. 30 calendar days
D. The next quarterly or annual report
C
If a device failure is occurring with greater than expected frequency and investigation of the problem
implicates improper use by the end user, which of the following typically occurs?
A. The labeling is revised.
B. The product is recalled.
C. The product is redesigned.
D. A "Dear Doctor" letter is issued.
A
, You have modified your 510(k) cleared device with a special 510(k). In which of the following cases
would you need to create a new listing for the device?
A. You have added new sizes and shapes in the product portfolio.
B. You have changed the material composition of the device.
C. You have changed the package of the device.
D. None of the above.
D
According to the QSR, when an investigation of a complaint is conducted all of the following are
requirements for inclusion in the record of the investigation EXCEPT:
A. The dates and results of the investigation
B. The nature and details of the complaint
C. Changes in procedures correcting quality problems
D. Any reply to the complainant
C
The QSR calls for the manufacturer of finished devices to carry out all of the following EXCEPT:
A. Conduct quality audits by individuals who do not have direct responsibility for the operation being
audited
B. Audit operations annually
C. Document the dates and results of quality audits and re-audits
D. Have findings reviewed by management responsible for the matters audited
B
Which of the following subsystems is NOT required by FDA in order to implement and maintain a Quality
System?
A. Production and process controls
B. Test and control article characterization
C. Packaging and labeling controls
D. Facility and equipment controls
B
A company wants to modify its legally marketed device such that the modification does not affect the
intended use or alter the fundamental scientific technology of the device. If the design outputs of the
modified device meet the design input requirements, this change would be best filed as a(n):
A. Special 510(k)
Questions and Verified Correct Answers JUST
RELEASED
A handling and storage system for medical devices must always include:
A. Procedures for rotation of stock
B. Separate rooms or cages for release and quarantine products
C. Procedures for receipt and transfer of product
D. Environmentally controlled areas for products with shelf life
C
Which of the following is exempt from GMP/QSR regulations?
A. Remanufacturers
B. Custom device manufacturers
C. Repackagers
D. Component manufacturers
D
Which division would have primary jurisdiction over a vascular graft with an antibiotic based on primary
mode of action?
A. CDER
B. CBER
C. CDRH
D. OCP
C
According to the Quality System Regulations, re-testing and re-evaluation of nonconforming devices
after rework activities must be documented in the:
A. Device history record
B. Device master record
C. Quality manual
D. Design history file
A
,Under the statutory violations, failure to meet 510(k) requirements for a device that is required to have
a 510(k) and is in commercial distribution is considered to be:
A. Adulteration.
B. Improper use
C. Misbranded
D. Fraudulent
C
A company's competitor is marketing a Class II suture which dissolves during the third week of use. The
company's current product has to be removed by a physician. However, a change in weaving
configuration gives this product the same dissolving time as the competitor's. When can the company's
new suture be marketed?
A. This requires a new 510(k) since significant change in product instructions might
affect efficacy.
B. After submission in a periodic report
C. After reporting clinical studies in an annual report
D. After submission of labeling change
A
A physician reports to a manufacturer that a patient was hospitalized with acute sepsis after treatment
with an approved device. This side effect is not listed in the package insert. This event must be reported
by the manufacturer to FDA no later than:
A. 5 calendar days
B. 15 calendar days
C. 30 calendar days
D. The next quarterly or annual report
C
If a device failure is occurring with greater than expected frequency and investigation of the problem
implicates improper use by the end user, which of the following typically occurs?
A. The labeling is revised.
B. The product is recalled.
C. The product is redesigned.
D. A "Dear Doctor" letter is issued.
A
, You have modified your 510(k) cleared device with a special 510(k). In which of the following cases
would you need to create a new listing for the device?
A. You have added new sizes and shapes in the product portfolio.
B. You have changed the material composition of the device.
C. You have changed the package of the device.
D. None of the above.
D
According to the QSR, when an investigation of a complaint is conducted all of the following are
requirements for inclusion in the record of the investigation EXCEPT:
A. The dates and results of the investigation
B. The nature and details of the complaint
C. Changes in procedures correcting quality problems
D. Any reply to the complainant
C
The QSR calls for the manufacturer of finished devices to carry out all of the following EXCEPT:
A. Conduct quality audits by individuals who do not have direct responsibility for the operation being
audited
B. Audit operations annually
C. Document the dates and results of quality audits and re-audits
D. Have findings reviewed by management responsible for the matters audited
B
Which of the following subsystems is NOT required by FDA in order to implement and maintain a Quality
System?
A. Production and process controls
B. Test and control article characterization
C. Packaging and labeling controls
D. Facility and equipment controls
B
A company wants to modify its legally marketed device such that the modification does not affect the
intended use or alter the fundamental scientific technology of the device. If the design outputs of the
modified device meet the design input requirements, this change would be best filed as a(n):
A. Special 510(k)
