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Ronvig A/S

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K032925B&R DEVICEDecember 22, 2003
K010816DENTO-PREP PARTICLE MICROBLASTERMay 10, 2001