Hasomed GmbH is one of 491 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Hasomed GmbH - FDA 510(k) Cleared Devices
Recent clearances: RehaStim 2, REHASTIM 2, ERIGOPRO (FES), REHASTIM 2, REHAMOVE 2
4
Total
4
Cleared
0
Denied
Hasomed GmbH has 4 FDA 510(k) cleared medical devices. Based in Magdeburg, DE.
Historical record: 4 cleared submissions from 2007 to 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Hasomed GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hasomed GmbH
4 devices