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Guidance Documents/Guidance-Document/Deciding When to Submit a 510(k) for a Software Change to an Existing Device: Guidance for Industry and Food and Drug Administration Staff

Deciding When to Submit a 510(k) for a Software Change to an Existing Device: Guidance for Industry and Food and Drug Administration Staff

Detailed guidance document from FDA and regulatory agencies.

Document Details

Guidance Document

October 25, 2017

March 2, 2020

Center for Devices and Radiological Health

303c36a0-3191-4197-bc16-584e24525d07

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