Pentapharm GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Pentapharm GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Pentapharm GmbH has 1 FDA 510(k) cleared medical devices. Based in Munich, DE.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Pentapharm GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pentapharm GmbH
1 devices