Capillus302, Capillus312, Capillus352

Capillus302, Capillus312, Capillus352 is an FDA 510(k)-cleared medical device (K162994) manufactured by Capillus, LLC. 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 November 17, 2016. Regulation: 8.