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. Ophthalmic ✕
4 devices
Cleared
Dec 14, 1988
SLT CONTACT LASER SYSTEM CYCLOPHOTOCOAGULATION
Ophthalmic
169d
Cleared
Sep 30, 1988
SLT CL60 CONTACT LASER SYSTEM, CUTTING & COAGULA.
Ophthalmic
80d
Cleared
Sep 26, 1988
SLT CONTACT LASER SYSTEM ENDOPHOTOCOAGULATION
Ophthalmic
104d
Cleared
Jun 06, 1988
SLT CONTACT LASER SYSTEM OCULOPLASTICS
Ophthalmic
82d