
Skytron, Div. the Kmw Group, Inc.
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SKYTRON MODEL 1100 AND MODEL 142 is an FDA 510(k)-cleared medical device (K900290) 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 February 19, 1990. Regulation: 8.