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Surgical Laser Technologies, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
51
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K042211MODIFICATION TO: LASERPRO 810, 940, AND 980 DIODE DIODE LASER SYSTEMSNovember 8, 2004
K023624SLT VENOUS FIBER DELIVERY SYSTEMS, MODEL: 0041-6772/0041-6781/0041-6752/0041-6761/0041-6912/0041-692January 27, 2003
K011409SLT LASERPRO CTH HOLMIUM LASER SYSTEMJune 14, 2001
K010041SLT DIFFUSER FIBERMarch 7, 2001
K984018HEMOSLEEVE, MODEL 4.0MM, 5.5MMMarch 15, 1999
K983050PNEUMATIC CUTTER SYSTEMNovember 25, 1998
K981041SLT BIPOLAR SHEATHAugust 27, 1998
K972548SLT CL MD CONTACT LASER SYSTEMApril 21, 1998
K980156SLT SELECT FIBER DELIVERY SYSTEM AND CONTACT TIPSFebruary 27, 1998
K960821SLT FUMICH PROBE GUIDEMay 16, 1996
K954727SLT MULTIDIMENSIONAL CONTACT LASER SYSTEM (MODIFICATION)February 5, 1996
K952661SLT THERMALITE DIODE LASER SERIES, DIODE 980, 810, 940October 6, 1995
K952605SUCTION/IRRIGATOR TUBING KITSeptember 15, 1995
K952216SLT MULTIDIMENSIONAL CONTACT LASER SYSTEM & WCE DIFFUSER FLAT PROBE DF 2August 18, 1995
K952754SACS, INDEPENDENT FIBER COOLANT SYSTEMJuly 31, 1995
K952813SLT MULTIDIMENSIONAL CONTACT LASER SYSTEMJuly 20, 1995
K931490SLT MULTIDIMENSIONAL CONTACT LASER SYSTEM FAMILYMay 5, 1995
K950819SLT SIDEFIRING REFRACTIVE FIBER (HIGH POWER DENSITY FIBER)April 18, 1995
K931286SLT MULTIDIMENSIONAL CONTACT LASER SYSTEMFebruary 6, 1995
K934208SLT PRISM/REFRACTING PROBEAugust 26, 1994