
Light Sources, Inc.
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U.V. SUNLAMP 95UF-11 is an FDA 510(k)-cleared medical device (K870167) manufactured by Light Sources, 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 February 8, 1987. Regulation: 8.