
Skytron, Div. the Kmw Group, Inc.
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SKYTRON ELITE 6000 & 6001 SURGICAL TABLES is an FDA 510(k)-cleared medical device (K853480) 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 September 11, 1985. Regulation: 8.