TEC PORTAMAX H.V. PULSED GALVANIC STIMULATOR

TEC PORTAMAX H.V. PULSED GALVANIC STIMULATOR is an FDA 510(k)-cleared medical device (K861739) manufactured by J.A. Preston Corp.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 8, 1986. Regulation: 8.