American Laser Corp.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K010046NUVOLASE 532 MEDICAL LASER SYSTEMApril 5, 2001
K990665BQ/BM INTEGRATED LASER DELIVERY SYSTEMMay 17, 1999
K990725NUVOLASE 532 LASER SYSTEMMarch 22, 1999
K827819LASER PHOTOCOAGULATORJanuary 7, 1983
K813429LASER PHOTOCOAGULATOR ARGON MED. LASERJanuary 22, 1982