PULSETTE 110 TRANSCUTANEOUS ELEC-NERVE

PULSETTE 110 TRANSCUTANEOUS ELEC-NERVE is an FDA 510(k)-cleared medical device (K830792) manufactured by Bomed Medical Mfr., 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 March 28, 1983. Regulation: 8.