PRE-GELLED DISPOS ELECTRODE

PRE-GELLED DISPOS ELECTRODE is an FDA 510(k)-cleared medical device (K832877) manufactured by Advance Tech Intl.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 21, 1983. Regulation: 8.