ELECTROTRACE DISPOSABLE AG/AGCL EKG MON. ELEC.

ELECTROTRACE DISPOSABLE AG/AGCL EKG MON. ELEC. is an FDA 510(k)-cleared medical device (K903555) manufactured by Jason Marketing Co.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 4, 1990. Regulation: 8.