
Premier Laser Systems, Inc.
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AURORA SURGICAL DIODE LASER SYSTEM W/ACCESSORIES is an FDA 510(k)-cleared medical device (K954316) manufactured by Premier 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 December 14, 1995. Regulation: 8.