Medical Device Manufacturer · SE , Goteborg

Ascom (Sweden) AB - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2011

Total

Cleared

Denied

Ascom (Sweden) AB has 2 FDA 510(k) cleared medical devices. Based in Goteborg, SE.

Historical record: 2 cleared submissions from 2011 to 2018. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Ascom (Sweden) AB Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ascom (Sweden) AB

2 devices

1-2 of 2