Schwarzer 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
Schwarzer GmbH has 1 FDA 510(k) cleared medical devices. Based in Munich, DE.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Schwarzer GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Schwarzer GmbH
1 devices