
Intra Lase Corp.
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INTRALASE 600C LASER KERATOME is an FDA 510(k)-cleared medical device (K993153) manufactured by Intra Lase Corp.. 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 December 16, 1999. Regulation: 8.