Medical Device Manufacturer · US , Columbia City , IN

Tempo Technology, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1990

Total

Cleared

Denied

Tempo Technology, Inc. has 3 FDA 510(k) cleared medical devices. Based in Columbia City, US.

Historical record: 3 cleared submissions from 1990 to 1996. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Tempo Technology, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Tempo Technology, Inc.

3 devices

1-3 of 3