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

Clearance record K140903

NUVIS ARTHROSCOPE · Integrated Endoscopy, Inc. · decided 2014-07-17 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Nuvis140-4010-1INTEGRATED ENDOSCOPY, INC.HRX08538160080010