Medical Device Manufacturer · US , City Of Industry , CA

Teledyne Electronic Technologies - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1999

Total

Cleared

Denied

Teledyne Electronic Technologies has 2 FDA 510(k) cleared medical devices. Based in City Of Industry, US.

Historical record: 2 cleared submissions from 1999 to 2000. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Teledyne Electronic Technologies Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Teledyne Electronic Technologies

2 devices

1-2 of 2