Metek GmbH is one of 507 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Metek GmbH - FDA 510(k) Cleared Devices
Recent clearances: MASSAGE MATTRESS VM9100RM
1
Total
1
Cleared
0
Denied
Metek GmbH has 1 FDA 510(k) cleared medical devices. Based in Leinefelde, DE.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Metek GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Metek GmbH
1 devices