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Dpm USA Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
3
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K090055
LOW & HIGH SPEED KIT
October 27, 2009
K083059
AIR SONIC SCALER
January 30, 2009