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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K211654

Penumbra System (Reperfusion Catheter RED 72) · Penumbra, Inc. · decided 2021-08-16 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
RED 72RED72SDKIT-APENUMBRA, INC.NRY00815948025943