
Cabot Medical Corp.
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SYSTEM 3000 XENON VIDEOLAP LIGHT is an FDA 510(k)-cleared medical device (K923210) manufactured by Cabot Medical Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 4, 1992. Regulation: 8.