Medical Device Manufacturer · US , Iowa City , IA

Titronics Medical Instruments, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1990

Total

Cleared

Denied

Titronics Medical Instruments, Inc. has 2 FDA 510(k) cleared medical devices. Based in Iowa City, US.

Historical record: 2 cleared submissions from 1990 to 1993. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Titronics Medical Instruments, Inc.

2 devices

1-2 of 2