
Kirschner Medical Corp.
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MEDICAM 900 AUTOELECTRONIC LIGHT SOURCE is an FDA 510(k)-cleared medical device (K922544) manufactured by Kirschner Medical Corp.. 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 August 6, 1992. Regulation: 8.