Medical Device Manufacturer · US , Mchenry , IL

Squibb Diagnostics - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1983

Total

Cleared

Denied

Squibb Diagnostics has 3 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 3 cleared submissions from 1983 to 1989.

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

Squibb Diagnostics 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 - Squibb Diagnostics

3 devices

1-3 of 3