Medical Device Manufacturer · DE , Luebeck

Asap Endoscopic Products GmbH - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2003
5
Total
5
Cleared
0
Denied

Asap Endoscopic Products GmbH has 5 FDA 510(k) cleared medical devices. Based in Luebeck, DE.

Historical record: 5 cleared submissions from 2003 to 2013. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Asap Endoscopic Products GmbH Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Asap Endoscopic Products GmbH
5 devices
1-5 of 5
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