
M.P. Video, Inc.
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ML-800 AUTOELECTRONIC LIGHT SOURCE is an FDA 510(k)-cleared medical device (K893828) manufactured by M.P. Video, 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 23, 1989. Regulation: 8.