VALLEY FORGE SCIEN-TENS UNIT & ACCESS. LEAD WIRE &

VALLEY FORGE SCIEN-TENS UNIT & ACCESS. LEAD WIRE & is an FDA 510(k)-cleared medical device (K853992) manufactured by Valley Forge Scientific Corp.. 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 20, 1986. Regulation: 8.