Maquet GmbH and Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Maquet GmbH and Co. KG - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Maquet GmbH and Co. KG has 1 FDA 510(k) cleared medical devices. Based in Rastatt De-Bw, DE.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Maquet GmbH and Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Maquet GmbH and Co. KG
1 devices