
Light Sources, Inc.
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U.V. SUNLAMP (U.V. LIGHT, DERMATOLOGIC) is an FDA 510(k)-cleared medical device (K900693) 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 March 26, 1990. Regulation: 8.