
Heraeus Lasersonics, Inc.
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CROSSFIRE LASER ASSISTED ASPIRATION CANNULA is an FDA 510(k)-cleared medical device (K911408) manufactured by Heraeus Lasersonics, 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 June 2, 1991. Regulation: 8.