
Hgm, Inc.
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ENDOCOAGULATOR MODELS 8 AND 20 ARGON LASER is an FDA 510(k)-cleared medical device (K873773) manufactured by Hgm, 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 12, 1987. Regulation: 8.