RAC (Devices) Practice Questions - Regulatory Affairs Certification - Devices Exam

Under the US FDA risk-based framework, into how many regulatory classes are medical devices categorized?

Three (Class I, II, and III) Two (Class A and Class B) Four (Class I, IIa, IIb, and III) Five (Class 1 through 5)

Correct Answer:

Three (Class I, II, and III)

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