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

Clearance record K201058

Accuvue+ · Radmedix, LLC · decided 2020-05-06 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Radmedix AccuVue+5RADMEDIX, LLCLLZ00810035220379