Schwarzer Cardiotek GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Schwarzer Cardiotek GmbH - FDA 510(k) Cleared Devices
Recent clearances: EP-TRACER System
1
Total
1
Cleared
0
Denied
Schwarzer Cardiotek GmbH has 1 FDA 510(k) cleared medical devices. Based in Heilbronn, DE.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Schwarzer Cardiotek GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Graematter, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Schwarzer Cardiotek GmbH
1 devices