Medical Device Manufacturer · US , Albuquerque , NM

Rotek Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1987

Total

Cleared

Denied

Rotek Corp. has 2 FDA 510(k) cleared medical devices. Based in Albuquerque, US.

Historical record: 2 cleared submissions from 1987 to 1991. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Rotek Corp.

2 devices

1-2 of 2