Surgical Laser Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MODIFICATION TO: LASERPRO 810, 940, AND 980 DIODE DIODE LASER SYSTEMS, SLT VENOUS FIBER DELIVERY SYSTEMS, MODEL: 0041-6772/0041-6781/0041-6752/0041-6761/0041-6912/0041-6921, SLT LASERPRO CTH HOLMIUM LASER SYSTEM
51
Total
51
Cleared
0
Denied
FDA 510(k) Regulatory Record - Surgical Laser Technologies, Inc. General & Plastic Surgery ✕
36 devices
Cleared
Nov 08, 2004
MODIFICATION TO: LASERPRO 810, 940, AND 980 DIODE DIODE LASER SYSTEMS
General & Plastic Surgery
84d
Cleared
Jan 27, 2003
SLT VENOUS FIBER DELIVERY SYSTEMS, MODEL:...
General & Plastic Surgery
90d
Cleared
Jun 14, 2001
SLT LASERPRO CTH HOLMIUM LASER SYSTEM
General & Plastic Surgery
37d
Cleared
Mar 07, 2001
SLT DIFFUSER FIBER
General & Plastic Surgery
61d
Cleared
Mar 15, 1999
HEMOSLEEVE, MODEL 4.0MM, 5.5MM
General & Plastic Surgery
123d
Cleared
Apr 21, 1998
SLT CL MD CONTACT LASER SYSTEM
General & Plastic Surgery
287d
Cleared
Feb 27, 1998
SLT SELECT FIBER DELIVERY SYSTEM AND CONTACT TIPS
General & Plastic Surgery
42d
Cleared
May 16, 1996
SLT FUMICH PROBE GUIDE
General & Plastic Surgery
77d
Cleared
Feb 05, 1996
SLT MULTIDIMENSIONAL CONTACT LASER SYSTEM (MODIFICATION)
General & Plastic Surgery
143d
Cleared
Oct 06, 1995
SLT THERMALITE DIODE LASER SERIES, DIODE 980, 810, 940
General & Plastic Surgery
116d
Cleared
Aug 18, 1995
SLT MULTIDIMENSIONAL CONTACT LASER SYSTEM & WCE DIFFUSER FLAT PROBE DF 2
General & Plastic Surgery
99d
Cleared
Jul 31, 1995
SACS, INDEPENDENT FIBER COOLANT SYSTEM
General & Plastic Surgery
46d