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

Clearance record K210917

Single Use Injection Needle · Anrei Medical (Hangzhou) Co., Ltd. · decided 2021-05-28 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
AnreiNE-C2508Anrei Medical(HZ) Co.,Ltd.FBK06926839809147
AnreiNE-C2308Anrei Medical(HZ) Co.,Ltd.FBK06926839809161
AnreiNE-C2536Anrei Medical(HZ) Co.,Ltd.FBK06926839809130
AnreiNE-C2336Anrei Medical(HZ) Co.,Ltd.FBK06926839809154