MENTOR ACTIVATOR NEUROMUSCULAR STIMU

MENTOR ACTIVATOR NEUROMUSCULAR STIMU is an FDA 510(k)-cleared medical device (K820168) manufactured by Mentor Corp.. 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 February 23, 1982. Regulation: 8.