UNI-PULS(TENS) MODEL #292

UNI-PULS(TENS) MODEL #292 is an FDA 510(k)-cleared medical device (K865063) manufactured by Oms Medico, 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 March 16, 1987. Regulation: 8.