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Laser Industries , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
20
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K933362SHARPLAN CO2 SURGICAL LASERApril 7, 1994
K894765SHARPLAN SMOKE EVACUATION UNIT, MODEL 100September 28, 1989
K850633SHARPLAN MODEL 1060 CO/2 SURGICAL LASERAugust 7, 1985
K850628SHARPLAN 1040 CO/2 SURGICAL LASERAugust 7, 1985
K842997LASER RECTOSCOPE SET 784August 27, 1984
K832550SHARPLAN #734 LASER SURGICAL UNITApril 25, 1984
K832551SHARPLAN #745 LASER SURG. UNITApril 23, 1984
K832316OPHTHALMIC ARGON LASER #700AJanuary 30, 1984
K837573SHARPLAN LASER POSITIONING SYSTEMJune 28, 1983
K837342SHARPLAN 721 CO2 SURGICAL LASERMay 18, 1983
K837081MICROSCAN 771 MANIPULATORMarch 9, 1983
K828056MODEL 716 MICROMANIPULATORJanuary 6, 1983
K828194LASER LAPAROSCOPEOctober 5, 1982
K827607MODEL 712 MICROMANIPULATORJuly 22, 1982
K820101SHARPLAN 720 CO2 SURGICAL LASERFebruary 24, 1982
K801624SHARPLAN 723 CO2 LASER SURGICAL SYSTEMAugust 20, 1980
K792418SHARPLAN 743, CO2 LASER SURGICAL SYSTEMFebruary 5, 1980
K790526LIO-714 OPACITYMETERNovember 16, 1979
K782030LASER SYSTEM, SHARPLAN 791/HE, CO2January 22, 1979
K780585SURGICAL LASERJuly 19, 1978