STIMUPLEX, NERVE STIMULATOR

STIMUPLEX, NERVE STIMULATOR is an FDA 510(k)-cleared medical device (K860126) manufactured by Burron Medical Products, 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 February 27, 1986. Regulation: 8.