Medical Device Manufacturer · SE , Lund

Dignitana AB - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 2015

Total

Cleared

Denied

Dignitana AB has 1 FDA 510(k) cleared medical devices. Based in Lund, SE.

Historical record: 1 cleared submissions from 2015 to 2017. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Dignitana AB

2 devices

1-2 of 2