NERVE STIMULATOR, DIGITAL PERIPHERAL

NERVE STIMULATOR, DIGITAL PERIPHERAL is an FDA 510(k)-cleared medical device (K791047) manufactured by C.R. Bard, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 12, 1979. Regulation: 8.