MODEL 811 VERI/TENS & PO

MODEL 811 VERI/TENS & PO is an FDA 510(k)-cleared medical device (K840098) manufactured by Verite. 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 16, 1984. Regulation: 8.