Schwartz Electro-Optics, Inc.
Schwartz Electro-Optics, Inc. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 1998.
Top product codes for Schwartz Electro-Optics, Inc.
Recent clearances by Schwartz Electro-Optics, Inc.
- K980710 — SCHWARTZ ELECTRO-OPTICS, INC. CRYSTALASE 755 DP ALEXANDRITE LASER SYSTEM
- K980313 — SCHWARTZ ELECTRO-OPTICS, INC. CLR 2940 ERBIUM CRYSTALASE
- K973867 — SCHWARTZ ELECTRO-OPTICS, INC. CRYSTALASE 755 LASER SYSTEM
- K974039 — SCHWARTZ ELECTRO-OPTICS, INC. CLR 2940 ERBIUM CRYSTALASE
- K973603 — SCHWARTZ ELECTRO-OPTICS, INC. CRYSTALASE 1064/532 LASER SYSTEM
- K971404 — SCHWARTZ ELECTRO-OPTICS, INC. CLR 2940/ERBIUM CRYSTALASE (FORMERLY TRILASE 2940 ERBIUM LASER
- K953585 — SCHWARTZ ELECTRO-OPTICES, INC. TRILASE 2100/20 HOLMIUM LASER
- K954013 — TRILASE 2940 ERBIUM LASER
- K952554 — SCHWARTZ ELECTRO-OPTICS, INC. TRILASE LASER SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.