
Welch Allyn, Inc.
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CP100 & 200 12-LEAD RESTING ELECTROCARDIOGRAPHS is an FDA 510(k)-cleared medical device (K072449) manufactured by Welch Allyn, Inc.. 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 28, 2007. Regulation: 8.