Medical Device Manufacturer · US , Gaithersburg , MD

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

1 submissions · 1 cleared · Since 2003

Total

Cleared

Denied

Telemis S.A. has 1 FDA 510(k) cleared medical devices. Based in Gaithersburg, US.

Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Radiology.

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

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

1 devices

1-1 of 1