PROFESSIONAL MARK I BIOFEEDBACK SYS

PROFESSIONAL MARK I BIOFEEDBACK SYS is an FDA 510(k)-cleared medical device (K823381) manufactured by Srs Co.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 4, 1983. Regulation: 8.