Minnesota Laser Corp.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K874253ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA.July 12, 1988
K874255ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI.July 12, 1988
K874254ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONSMarch 4, 1988
K854473PORTALASE 300 CARBON DIOXIDE SURG LASER NEUROLOGICJune 20, 1986
K854468PORTALASE 200 CARBON DIOXIDE SURG LASER NEUROLOGICJune 20, 1986
K854471PORTALASE 300 CARBON DIOXIDE SURG LASER EAR/NOSE/TFebruary 13, 1986
K854472PORTALASE 300 CARBON DIOXIDE SURG LASER DERMATOLOGFebruary 11, 1986
K854469PORTALASE 200 CARBON DIOXIDE SURG LASER DERMATOLOGFebruary 11, 1986
K854470PORTALASE 300 CARBON DIOXIDE SURG LASER GYNECOLOGIFebruary 7, 1986
K852694PORTALASE 200 CARBON SURGICAL LASER SYSTEMSeptember 30, 1985
K852696FOR USE IN GENERAL & PLASTIC SURGERY & DERMATOLOGYSeptember 19, 1985
K852695FOR USE IN EAR; NOSE & THROAT MICROSURGERYAugust 30, 1985