FDA Device Info: IVC Filter 510k Decision Memos

FDA Device Info: IVC Filter 510k Decision Memos

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The full 510(k) decision memos for all IVC filters (78 510(k) clearances) of devices under the product code DTK (Filter, Intravascular, Cardiovascular).[REQ YEAR: 2023]

NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.

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