
Laser Photonics, Inc.
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LPI YAG MODEL 1003 SURGICAL LASER SYSTEM is an FDA 510(k)-cleared medical device (K900837) manufactured by Laser Photonics, 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 July 11, 1990. Regulation: 8.