Medical Device Manufacturer · CN , Beijing

Lepu Medical Technology (Beijing) Co., Ltd. - FDA 510(k) Cleared Devi...

7 submissions · 6 cleared · Since 2011

Recent clearances: Type I, Type II, Type III, Type IV, Shoocin Introducer Kit, ULTRASKIN HYDROPHILIC GUIDE WIRE

7
Total
6
Cleared
0
Denied

Lepu Medical Technology (Beijing) Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Beijing, CN.

Historical record: 6 cleared submissions from 2011 to 2018. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Lepu Medical Technology (Beijing) Co., Ltd. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by FDA Regulatory and Quality Systems Consultant and Vascular Solutions, Inc..

FDA 510(k) Regulatory Record - Lepu Medical Technology (Beijing) Co., Ltd.

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