Medical Device Manufacturer · US , Burbank , CA

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

4 submissions · 4 cleared · Since 2002

Total

Cleared

Denied

Limerick, Inc. has 4 FDA 510(k) cleared medical devices. Based in Burbank, US.

Historical record: 4 cleared submissions from 2002 to 2015. Primary specialty: Obstetrics & Gynecology.

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

Limerick, Inc. is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Limerick, Inc. — FDA 510(k) Products and Clearance History

4 devices

1-4 of 4