Capillus 112, Capillus 244

Capillus 112, Capillus 244 is an FDA 510(k)-cleared medical device (K192012) manufactured by Capillus. 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 11, 2019. Regulation: 8.