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General Project S.R.L.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
2
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K161502MC1 PlusAugust 16, 2016
K091615MED CONTOURMay 6, 2010
K062312AXIOM PULSED LIGHT SYSTEMOctober 16, 2006
K053041MED SCULPTAugust 2, 2006
K051508MED FLASH II INTENSE PULSED LIGHT SYSTEM.October 5, 2005
K004014MD 30 COMPACTMarch 16, 2001