TENS DEVICE FOR RELIEF OF CHRONIC PAIN, MODIFIED

TENS DEVICE FOR RELIEF OF CHRONIC PAIN, MODIFIED is an FDA 510(k)-cleared medical device (K924876) manufactured by Graham-Field, 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 February 28, 1994. Regulation: 8.