MDE ESCORT 1000 & MDE ESCOR 2000

MDE ESCORT 1000 & MDE ESCOR 2000 is an FDA 510(k)-cleared medical device (K842716) 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 February 7, 1985. Regulation: 8.