
Cardionet, Inc.
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CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL 1002 is an FDA 510(k)-cleared medical device (K052240) manufactured by Cardionet, 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 October 18, 2005. Regulation: 8.