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

Clearance record K193380

CERENOVUS Large Bore Catheter; CERENOVUS Aspiration Tubing Set · Codman & Shurtleff, Inc. · decided 2020-07-20 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
CERENOVUSEVT110Cerenovus, Inc.NRY10886704084563