
Skytron, Div. the Kmw Group, Inc.
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SKYTRON SKYBOOM SERIES is an FDA 510(k)-cleared medical device (K950192) manufactured by Skytron, Div. the Kmw Group, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 2, 1995. Regulation: 8.