FDA 510(k) Applications Submitted by SCHWARTZ ELECTRO-OPTICS, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K980313 |
01/27/1998 |
SCHWARTZ ELECTRO-OPTICS, INC. CLR 2940 ERBIUM CRYSTALASE |
SCHWARTZ ELECTRO-OPTICS, INC. |
K980710 |
02/24/1998 |
SCHWARTZ ELECTRO-OPTICS, INC. CRYSTALASE 755 DP ALEXANDRITE LASER SYSTEM |
SCHWARTZ ELECTRO-OPTICS, INC. |
K971404 |
04/16/1997 |
SCHWARTZ ELECTRO-OPTICS, INC. CLR 2940/ERBIUM CRYSTALASE (FORMERLY TRILASE 2940 ERBIUM LASER |
SCHWARTZ ELECTRO-OPTICS, INC. |
K953585 |
08/01/1995 |
SCHWARTZ ELECTRO-OPTICES, INC. TRILASE 2100/20 HOLMIUM LASER |
SCHWARTZ ELECTRO-OPTICS, INC. |
K954013 |
08/25/1995 |
TRILASE 2940 ERBIUM LASER |
SCHWARTZ ELECTRO-OPTICS, INC. |
K973603 |
09/22/1997 |
SCHWARTZ ELECTRO-OPTICS, INC. CRYSTALASE 1064/532 LASER SYSTEM |
SCHWARTZ ELECTRO-OPTICS, INC. |
K973867 |
09/22/1997 |
SCHWARTZ ELECTRO-OPTICS, INC. CRYSTALASE 755 LASER SYSTEM |
SCHWARTZ ELECTRO-OPTICS, INC. |
K974039 |
10/16/1997 |
SCHWARTZ ELECTRO-OPTICS, INC. CLR 2940 ERBIUM CRYSTALASE |
SCHWARTZ ELECTRO-OPTICS, INC. |
|
|