Medical Device Manufacturer · US , Hudson , NH

Tecme S.A. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2010

Total

Cleared

Denied

Tecme S.A. has 2 FDA 510(k) cleared medical devices. Based in Hudson, US.

Historical record: 2 cleared submissions from 2010 to 2012. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Tecme S.A. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Tecme S.A.

2 devices

1-2 of 2