XENON LIGHT SOURCE FOR ENDOSCOPIC PROCEDURES

XENON LIGHT SOURCE FOR ENDOSCOPIC PROCEDURES is an FDA 510(k)-cleared medical device (K863986) manufactured by American Edwards Laboratories. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 30, 1986. Regulation: 8.