RHYTHMLINK INTERNATIONAL SUBDERMAL NEEDLE ELECTRODES

RHYTHMLINK INTERNATIONAL SUBDERMAL NEEDLE ELECTRODES is an FDA 510(k)-cleared medical device (K022914) manufactured by Rhythmlink International, LLC. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 19, 2002. Regulation: 8.