
Lca, Inc.
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THE HOOK-CURVED CLOSED END/ELECT FIBER LASER DELIV SYS is an FDA 510(k)-cleared medical device (K944091) manufactured by Lca, 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 October 6, 1994. Regulation: 8.