Medical Device Manufacturer · US , Chicago , IL

Sabratek Corp. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1992

Total

Cleared

Denied

Sabratek Corp. has 7 FDA 510(k) cleared medical devices. Based in Chicago, US.

Historical record: 7 cleared submissions from 1992 to 1999. Primary specialty: General Hospital.

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

Sabratek Corp. 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 - Sabratek Corp.

7 devices

1-7 of 7