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. Anesthesiology ✕
2 devices