
Trimedyne, Inc.
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OPTILASE YAG MODEL 1000 is an FDA 510(k)-cleared medical device (K895874) manufactured by Trimedyne, 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 January 2, 1990. Regulation: 8.