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Laser Media

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K872352FIBERLASE II ND:YAG LASER FOR TREAT OF MENORRHAGIADecember 30, 1987
K872351FIBERLASE II ND:YAG LASER FOR PULMONARY USEDecember 11, 1987
K872350FIBERLASE II ND:YAG LASER FOR GASTRO.&UROLOGY USEAugust 10, 1987
K872031UNI-FIBER NON-REPAIRABLE FIBER DELIVERY SYSTEMAugust 4, 1987
K863428SINGLE USE LASER FIBER DELIVERY SYSTEM FOR ND: YAGDecember 3, 1986
K863583CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASERNovember 24, 1986
K862444FIBERLASE 100 MEDICAL LASER SYS/ND:YAG MENORRHAGIASeptember 25, 1986
K860063ND:YAG LASER SINGLE USE FIBER DELIVERY SYSTEMFebruary 5, 1986
K855197FIBERLASE 100 ND: YAG MEDICAL LASER SYSTEMJanuary 21, 1986
K852798FIBERLASE 100 MEDICAL LASER SYSTEMJuly 29, 1985
K850509ND:YAG FIBERLASE 100 MEDICAL LASER SYSTEMApril 8, 1985
K844869FIBERLASE 100 MEDICAL LASER SYSTEMJanuary 14, 1985