PULSAR #B SINGLE CHANNEL TENS-PULSAR D

PULSAR #B SINGLE CHANNEL TENS-PULSAR D is an FDA 510(k)-cleared medical device (K831950) manufactured by Spembly Medical , Ltd.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 31, 1983. Regulation: 8.