
Phoenix U.V.A. , Ltd.
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PHOENIX U.V.A. SUNTAN BEDS is an FDA 510(k)-cleared medical device (K854594) manufactured by Phoenix U.V.A. , Ltd.. 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 January 29, 1986. Regulation: 8.