OMNIPROBE ELECTRICAL NERVE STIMULATOR

OMNIPROBE ELECTRICAL NERVE STIMULATOR is an FDA 510(k)-cleared medical device (K831147) manufactured by Omni Intl., 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 July 17, 1983. Regulation: 8.