Medical Device Manufacturer · US , Findley , MN

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

4 submissions · 4 cleared · Since 1994

Total

Cleared

Denied

Rescare , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Findley, US.

Historical record: 4 cleared submissions from 1994 to 1996. Primary specialty: Anesthesiology.

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

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

4 devices

1-4 of 4