Medical Device Manufacturer · US , Waukegan , IL

Carefusion 2200 - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2009

Total

Cleared

Denied

Carefusion 2200 has 2 FDA 510(k) cleared medical devices. Based in Waukegan, US.

Historical record: 2 cleared submissions from 2009 to 2010. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Carefusion 2200 Filter by specialty or product code using the sidebar.

Carefusion 2200 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 - Carefusion 2200

2 devices

1-2 of 2