MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEW

MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEW is an FDA 510(k)-cleared medical device (K001308) manufactured by Agilent Technologies. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 16, 2000. Regulation: 8.