
Philips Lighting Co.
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TL 20W/12/RS & TL 40W/12/RS is an FDA 510(k)-cleared medical device (K935840) 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 February 23, 1994. Regulation: 8.