
Hgm Medical Laser Systems, Inc.
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ENDOSCOPIC USES OF THE ARGON LASER IN GENERAL SURG is an FDA 510(k)-cleared medical device (K896314) manufactured by Hgm Medical Laser Systems, 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 May 9, 1990. Regulation: 8.