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

Clearance record K211156

CONVIVO In Vivo Pathology Suite · Carl Zeiss Meditec, AG · decided 2021-12-29 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Sterile Sheath for CONVIVO302732-0530-000Carl Zeiss Meditec AGGWG LLZ OWN04049539103413
CONVIVO6918Carl Zeiss Meditec AGGWG LLZ OWN04049539069184