
Cynosure, Inc.
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ASA 'M FAMILY' DIODE LASER, MODEL MI, MIX5, M6 is an FDA 510(k)-cleared medical device (K051922) manufactured by Cynosure, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 13, 2005. Regulation: 8.