Medical Device Manufacturer · US , Mccordsville , IN

Caradyne, Ltd. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1999

Total

Cleared

Denied

Caradyne, Ltd. has 5 FDA 510(k) cleared medical devices. Based in Mccordsville, US.

Historical record: 5 cleared submissions from 1999 to 2004. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Caradyne, Ltd.

5 devices

1-5 of 5