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Prevent Products, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K003284PHLEBOPUMP, MODEL 1000January 17, 2001
K952975ANKLE CALF EXERCISER PHLEBOPUMPSeptember 25, 1996
K942618ANKLE CALF EXERCISERJune 22, 1994