
Gibson'S Mfg. Corp.
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SUNTAN BOOTH is an FDA 510(k)-cleared medical device (K810796) manufactured by Gibson'S Mfg. 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 August 2, 1981. Regulation: 8.