Medical Device Manufacturer · US , Mchenry , IL

Squibb & Sons, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1976

Total

Cleared

Denied

Squibb & Sons, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 5 cleared submissions from 1976 to 1982. Primary specialty: Immunology.

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

Squibb & Sons, 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 - Squibb & Sons, Inc.

5 devices

1-5 of 5