Medical Device Manufacturer · DE , 12099 Berlin

Aap GmbH and Co. Betriebs KG - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1997
1
Total
1
Cleared
0
Denied

Aap GmbH and Co. Betriebs KG has 1 FDA 510(k) cleared medical devices. Based in 12099 Berlin, DE.

Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Aap GmbH and Co. Betriebs KG Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Aap GmbH and Co. Betriebs KG
1 devices
1-1 of 1
Filters
All1 Orthopedic 1