Medical Device Manufacturer · US , Edina , MN

Cardia Innovation AB - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2006

Total

Cleared

Denied

Cardia Innovation AB has 2 FDA 510(k) cleared medical devices. Based in Edina, US.

Historical record: 2 cleared submissions from 2006 to 2012. Primary specialty: Obstetrics & Gynecology.

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

Cardia Innovation AB is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cardia Innovation AB

2 devices

1-2 of 2