Medical Device Manufacturer · US , W St Paul , MN

Prevent Products, Inc.

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

Prevent Products, Inc. — FDA 510(k) Submissions

Prevent Products, Inc. has submitted 3 FDA 510(k) premarket notifications since 1994, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Exerciser, Powered, Sleeve, Limb, Compressible . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
Filters
Filter by Specialty
All3 Physical Medicine 2 Cardiovascular 1