
Skytron, Div. the Kmw Group, Inc.
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SKYTRON LIFE ISLAND 21 is an FDA 510(k)-cleared medical device (K926045) manufactured by Skytron, Div. the Kmw Group, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 26, 1993. Regulation: 8.

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