Medical Device Manufacturer · US , W St Paul , MN

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

3 submissions · 3 cleared · Since 1994
3
Total
3
Cleared
0
Denied

Prevent Products, Inc. has 3 FDA 510(k) cleared medical devices. Based in W St Paul, US.

Historical record: 3 cleared submissions from 1994 to 2001. Primary specialty: Physical Medicine.

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

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

3 devices
1-3 of 3
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