ESCORT-LINK ARRHYTHMIA OPTION 23L

ESCORT-LINK ARRHYTHMIA OPTION 23L is an FDA 510(k)-cleared medical device (K915153) manufactured by Medical Data Electronics. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 26, 1992. Regulation: 8.