Medical Device Manufacturer · US , Niagara Falls , NY

Cardon Rehabilitation Products, Inc. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1995
16
Total
16
Cleared
0
Denied

Cardon Rehabilitation Products, Inc. has 16 FDA 510(k) cleared physical medicine devices. Based in Niagara Falls, US.

Historical record: 16 cleared submissions from 1995 to 1996.

Browse the complete list of FDA 510(k) cleared physical medicine devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Cardon Rehabilitation Products, Inc.

16 devices
1-12 of 16
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