Mavig GmbH is one of 516 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Mavig GmbH has 1 FDA 510(k) cleared medical devices. Based in Munchen, DE.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Mavig 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 - Mavig GmbH
1 devices