American Laser Medical

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K990780NUVOLASE 532 CUTANEOUS LASER SYSTEMMarch 22, 1999
K972765NUVOLASE 720 SYSTEM FOR OPHTHALMOLOGY LASEROctober 21, 1997
K972561NUVOLASE 660 LASER SYSTEM FOR OPHTHALMOLOGYOctober 6, 1997
K970667NUVO-LASE 660 LASER SYSTEMMay 13, 1997
K963389FLEX-LASE 600 SERIES ION LASER SYSTEMNovember 26, 1996