FACEMASTER FACIAL TONING SYSTEM

FACEMASTER FACIAL TONING SYSTEM is an FDA 510(k)-cleared medical device (K040871) manufactured by Facemaster of Beverly Hills, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 31, 2005. Regulation: 8.