PHOTONOVA FAMILY OF PULSED LIGHT SYSTEMS

PHOTONOVA FAMILY OF PULSED LIGHT SYSTEMS is an FDA 510(k)-cleared medical device (K073477) manufactured by Photonova Ofsweden AB. 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 8, 2008. Regulation: 8.