Tom Medical Entwicklungs GmbH is one of 45 FDA 510(k) medical device manufacturers from Austria in the dataset, ranked by real submission volume.
Tom Medical Entwicklungs GmbH - FDA 510(k) Cleared Devices
Recent clearances: MEDILOGAR4, MEDILOGAR12
1
Total
1
Cleared
0
Denied
Tom Medical Entwicklungs GmbH has 1 FDA 510(k) cleared medical devices. Based in Graz, AT.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Tom Medical Entwicklungs GmbH 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 - Tom Medical Entwicklungs GmbH
1 devices