LaserCap300, LaserCap224, LaserCap120, LaserCap80

LaserCap300, LaserCap224, LaserCap120, LaserCap80 is an FDA 510(k)-cleared medical device (K161875) manufactured by Transdermal Cap, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 29, 2016. Regulation: 8.