ELECTRO-NERVE STIMULATOR HL

ELECTRO-NERVE STIMULATOR HL is an FDA 510(k)-cleared medical device (K841184) manufactured by Biomedical Life Systems, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 3, 1984. Regulation: 8.