
Schwartz Electro-Optics, Inc.
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SCHWARTZ ELECTRO-OPTICS, INC. CRYSTALASE 755 LASER SYSTEM is an FDA 510(k)-cleared medical device (K973867) manufactured by Schwartz Electro-Optics, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 9, 1998. Regulation: 8.