DUAL CHANNEL TENS, PULSAR REMOTE CONTRL

DUAL CHANNEL TENS, PULSAR REMOTE CONTRL is an FDA 510(k)-cleared medical device (K842888) manufactured by Cryomedics, 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 January 13, 1985. Regulation: 8.