
Dermatron Corp.
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SUNLAMP (F40-UVB & F20-UVB) is an FDA 510(k)-cleared medical device (K760482) manufactured by Dermatron Corp.. 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 September 14, 1976. Regulation: 8.