Medical Device Manufacturer · US , Washington , DC

Compex S.A. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2002
1
Total
1
Cleared
0
Denied

Compex S.A. has 1 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Compex S.A. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Compex S.A.

1 devices
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All1 Physical Medicine 1