Medical Device Manufacturer · US , Libertyville , IL

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

14 submissions · 14 cleared · Since 1996
14
Total
14
Cleared
0
Denied

Heelbo, Inc. has 14 FDA 510(k) cleared general hospital devices. Based in Libertyville, US.

Historical record: 14 cleared submissions from 1996 to 1998.

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

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

14 devices
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