Endo Lase, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
24
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K853900ENDO-LASE CD40 FOR NEUROSURGERYJune 18, 1986
K853878ENDO-LASE CD-100 CO2 LASER FOR NEUROSURGERYMay 2, 1986
K853876ENDO-LSE CD-100 CO2 LASER FOR GYNECOLOGYFebruary 21, 1986
K855093MEDILAS 2 ND:YAG LASER SURGERY SYSTEMFebruary 21, 1986
K853903ENDO-LASE CD40 CO2 FOR GYNECOLOGYFebruary 21, 1986
K853877ENDO-LASE CD-100 CO2 LASER FOR DERMATOLOGYFebruary 19, 1986
K853901ENDO-LASE CD 40 FOR DERMATOLOGYFebruary 19, 1986
K853580MEDILAS 2February 13, 1986
K860152MODEL 700 EVACUATOR FOR USE WITH LASER SURGERYFebruary 5, 1986
K853875ENDO-LASE CD-100 CO2 LASER FOR OTORHINOLARYNGOLOGYJanuary 9, 1986
K853902ENDO-LASE CD40 FOR OTORHINOLARYNGOLOGYJanuary 9, 1986
K853904ENDO-LASE CD40 FOR UROLOGYOctober 25, 1985
K853874ENDO-LASE CD-100 CO2 LASER FOR EXTERNAL GENITALIA-October 25, 1985
K852507ND: YAGLASER FOR PALLIATIVE TREAT OF OBSTRUCTIONJuly 5, 1985
K851527UTILIZATION OF ND:YAG LASER FOR TREATMENT RECTAL PMay 17, 1985
K844460ND. YAG LASER RECTAL PATHOLOGYJanuary 16, 1985
K844459ND:YAG LASER UROLOGICAL SURGERYJanuary 16, 1985
K844458ND:YAG LASER PULMONARY OBSTRUCTIONJanuary 3, 1985
K842810INFRARED COAGULATOROctober 18, 1984
K843293ND-YAG LASER FOR UROLOGICAL SURGERYOctober 2, 1984