Medical Device Manufacturer · US , West Hartford , CT

Transcor, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1987

Total

Cleared

Denied

Transcor, Inc. has 2 FDA 510(k) cleared medical devices. Based in West Hartford, US.

Historical record: 2 cleared submissions from 1987 to 1987. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Transcor, Inc.

2 devices

1-2 of 2