Medical Device Manufacturer · DE , Schwerin

Human Med AG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2008

Recent clearances: LIPCOLLECTOR II, BODY-JET

2
Total
2
Cleared
0
Denied

Human Med AG has 2 FDA 510(k) cleared medical devices. Based in Schwerin, DE.

Historical record: 2 cleared submissions from 2008 to 2010. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Human Med AG Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Tuv Sud America, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Human Med AG

2 devices
1-2 of 2
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