Medical Device Manufacturer · US , Sterling , VA

Tulan Corp. C/O Richard Hamer Assoc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1988

Total

Cleared

Denied

Tulan Corp. C/O Richard Hamer Assoc. has 2 FDA 510(k) cleared medical devices. Based in Sterling, US.

Historical record: 2 cleared submissions from 1988 to 1989. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Tulan Corp. C/O Richard Hamer Assoc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Tulan Corp. C/O Richard Hamer Assoc.

2 devices

1-2 of 2