Lasermatic, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K903131LASERMATIC SUPERCOMBO(TM) SURGICAL LASER SYSTEMFebruary 19, 1991
K901638MODIFIED COMBOLASER 5050 & NEW MODEL 5050 VER. 33June 27, 1990
K895279LASERMATIC COMBOLASER MODEL 5050November 8, 1989
K893529COMBOLASER MODEL 5050June 8, 1989
K871875MODEL 5050 SURGILASER FOR OB-GYN USEAugust 22, 1988
K870587LASERMATIC SURGILASER MODEL 5050August 10, 1988
K871934MODEL 5050 SURGILASER FOR GASTRO-INTESTINAL USEMarch 25, 1988
K871932MODEL 5050 SURGILASER FOR UROLOGY USEMarch 25, 1988
K871876MODEL 5050 SURGILASER FOR PULMONARY USEJanuary 22, 1988
K871933MODEL 5050 SURGILASER FOR NEUROSURGERY USEJanuary 22, 1988