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

Clearance record K120193

ANY VIEW PATIENT MONITORS · Guangdong Biolight Meditech Co., Ltd. · decided 2012-06-29 (SESE)

FDA 510(k) database ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Venni / Biolight A5VENNI INSTRUMENTS INC.MWI00852503007167