Medical Device Manufacturer · US , New Port Riche , FL

Te ME NA S.A.R.L. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1999

Total

Cleared

Denied

Te ME NA S.A.R.L. has 5 FDA 510(k) cleared medical devices. Based in New Port Riche, US.

Historical record: 5 cleared submissions from 1999 to 2001. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Te ME NA S.A.R.L. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Te ME NA S.A.R.L.

5 devices

1-5 of 5