Cryofos Medical GmbH is one of 490 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Cryofos Medical GmbH - FDA 510(k) Cleared Devices
Recent clearances: CRYOFOS
1
Total
1
Cleared
0
Denied
Cryofos Medical GmbH has 1 FDA 510(k) cleared medical devices. Based in Karlsruhe, DE.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Cryofos Medical GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tenssource, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Cryofos Medical GmbH
1 devices