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

Clearance record K191237

CERENOVUS Large Bore Catheter · Codman & Shurtleff, Inc. · decided 2019-11-08 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
(unnamed)IC71135UGMedos International SàrlDQY10886704082385
(unnamed)IC71125UGMedos International SàrlDQY10886704082361
(unnamed)IC71132UGMedos International SàrlDQY10886704082378