Schwartz Electro-Optics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SCHWARTZ ELECTRO-OPTICS, INC. CRYSTALASE 755 DP ALEXANDRITE LASER SYSTEM, SCHWARTZ ELECTRO-OPTICS, INC. CLR 2940 ERBIUM CRYSTALASE, SCHWARTZ ELECTRO-OPTICS, INC. CRYSTALASE 755 LASER SYSTEM
9
Total
9
Cleared
0
Denied
FDA 510(k) Regulatory Record - Schwartz Electro-Optics, Inc. General & Plastic Surgery ✕
9 devices
Cleared
May 22, 1998
SCHWARTZ ELECTRO-OPTICS, INC. CRYSTALASE 755 DP ALEXANDRITE LASER SYSTEM
General & Plastic Surgery
87d
Cleared
Mar 19, 1998
SCHWARTZ ELECTRO-OPTICS, INC. CLR 2940 ERBIUM CRYSTALASE
General & Plastic Surgery
51d
Cleared
Feb 10, 1998
SCHWARTZ ELECTRO-OPTICS, INC. CRYSTALASE 755 LASER SYSTEM
General & Plastic Surgery
141d
Cleared
Jan 12, 1998
SCHWARTZ ELECTRO-OPTICS, INC. CLR 2940 ERBIUM CRYSTALASE
General & Plastic Surgery
88d
Cleared
Dec 19, 1997
SCHWARTZ ELECTRO-OPTICS, INC. CRYSTALASE 1064/532 LASER SYSTEM
General & Plastic Surgery
88d
Cleared
Jul 09, 1997
SCHWARTZ ELECTRO-OPTICS, INC. CLR 2940/ERBIUM CRYSTALASE (FORMERLY TRILASE...
General & Plastic Surgery
84d
Cleared
Feb 05, 1996
SCHWARTZ ELECTRO-OPTICES, INC. TRILASE 2100/20 HOLMIUM LASER
General & Plastic Surgery
188d
Cleared
Jan 31, 1996
TRILASE 2940 ERBIUM LASER
General & Plastic Surgery
159d
Cleared
Aug 28, 1995
SCHWARTZ ELECTRO-OPTICS, INC. TRILASE LASER SYSTEM
General & Plastic Surgery
87d