Medical Device Manufacturer · US , North Chicago , IL

AbbVie, Inc. - FDA 510(k) Cleared Devices

6 submissions · 4 cleared · Since 2014

Total

Cleared

Denied

AbbVie, Inc. has 4 FDA 510(k) cleared medical devices. Based in North Chicago, US.

Historical record: 4 cleared submissions from 2014 to 2015. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by AbbVie, Inc. Filter by specialty or product code using the sidebar.

AbbVie, Inc. 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 - AbbVie, Inc.

6 devices

1-6 of 6