
Skytron, Div. the Kmw Group, Inc.
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STELLAR SERIES SURGICAL LIGHTS WITH HERMES is an FDA 510(k)-cleared medical device (K021585) manufactured by Skytron, Div. the Kmw Group, 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 November 12, 2002. Regulation: 8.