FDA 510(k) Applications Submitted by SURGICAL LASER TECHNOLOGIES, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K042211 |
08/16/2004 |
MODIFICATION TO: LASERPRO 810, 940, AND 980 DIODE DIODE LASER SYSTEMS |
SURGICAL LASER TECHNOLOGIES, INC. |
| K010041 |
01/05/2001 |
SLT DIFFUSER FIBER |
SURGICAL LASER TECHNOLOGIES, INC. |
| K011409 |
05/08/2001 |
SLT LASERPRO CTH HOLMIUM LASER SYSTEM |
SURGICAL LASER TECHNOLOGIES, INC. |
| K023624 |
10/29/2002 |
SLT VENOUS FIBER DELIVERY SYSTEMS, MODEL: 0041-6772/0041-6781/0041-6752/0041-6761/0041-6912/0041-6921 |
SURGICAL LASER TECHNOLOGIES, INC. |
| K980156 |
01/16/1998 |
SLT SELECT FIBER DELIVERY SYSTEM AND CONTACT TIPS |
SURGICAL LASER TECHNOLOGIES, INC. |
| K981041 |
03/20/1998 |
SLT BIPOLAR SHEATH |
SURGICAL LASER TECHNOLOGIES, INC. |
| K972548 |
07/08/1997 |
SLT CL MD CONTACT LASER SYSTEM |
SURGICAL LASER TECHNOLOGIES, INC. |
| K983050 |
09/01/1998 |
PNEUMATIC CUTTER SYSTEM |
SURGICAL LASER TECHNOLOGIES, INC. |
| K984018 |
11/12/1998 |
HEMOSLEEVE, MODEL 4.0MM, 5.5MM |
SURGICAL LASER TECHNOLOGIES, INC. |
| K960821 |
02/29/1996 |
SLT FUMICH PROBE GUIDE |
SURGICAL LASER TECHNOLOGIES, INC. |
| K954727 |
09/15/1995 |
SLT MULTIDIMENSIONAL CONTACT LASER SYSTEM (MODIFICATION) |
SURGICAL LASER TECHNOLOGIES, INC. |
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