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Guidance Documents/Guidance-Document/Determination of Intended Use for 510(k) Devices - Guidance for CDRH Staff (Update to K98-1)

Determination of Intended Use for 510(k) Devices - Guidance for CDRH Staff (Update to K98-1)

Detailed guidance document from FDA and regulatory agencies.

Document Details

Guidance Document

December 2, 2002

March 19, 2020

Center for Devices and Radiological Health

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