Medical Device Manufacturer · US , Mchenry , IL

Chesire Laboratories - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1977

Total

Cleared

Denied

Chesire Laboratories has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 4 cleared submissions from 1977 to 1993. Primary specialty: General Hospital.

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

Chesire Laboratories 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 - Chesire Laboratories

4 devices

1-4 of 4