Medical Device Manufacturer · US , Oxford , IA

Titronics Research & Development Co. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1998

Total

Cleared

Denied

Titronics Research & Development Co. has 2 FDA 510(k) cleared medical devices. Based in Oxford, US.

Historical record: 2 cleared submissions from 1998 to 2003. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Titronics Research & Development Co. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Titronics Research & Development Co.

2 devices

1-2 of 2