Te ME NA Sas is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Te ME NA Sas - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
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