Straub Medical AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Straub Medical AG - FDA 510(k) Cleared Devices
Recent clearances: Straub Endovascular System
1
Total
1
Cleared
0
Denied
Straub Medical AG has 1 FDA 510(k) cleared medical devices. Based in Wangs, CH.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Straub Medical AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Namsa as regulatory consultant.
FDA 510(k) Regulatory Record - Straub Medical AG
1 devices