
Philips Lighting Co.
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PHILIPS PLS9W/12/2P UVB is an FDA 510(k)-cleared medical device (K021514) manufactured by Philips Lighting Co.. 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 May 15, 2002. Regulation: 8.