MONTERIS MEDICAL AUTOLITT LASER PROBE

MONTERIS MEDICAL AUTOLITT LASER PROBE is an FDA 510(k)-cleared medical device (K081509) manufactured by Monteris Medical,. 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 April 30, 2009. Regulation: 8.