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

Clearance record K161763

Smith & Nephew TRUCLEAR ULTRA Mini Tissue Removal Device · Smith & Nephew, Inc. · decided 2016-11-22 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
TruClear72204064Covidien LPHIH10884521744097