Medical Device Manufacturer · US , Apollo Beach , FL

Te ME NA Sas - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2006

Total

Cleared

Denied

Te ME NA Sas has 2 FDA 510(k) cleared medical devices. Based in Apollo Beach, US.

Historical record: 2 cleared submissions from 2006 to 2008. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Te ME NA Sas

2 devices

1-2 of 2