
Monebo Technologies, Inc.
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MONEBO AUTOMATED ECG ANALYSIS AND INTERPRETATION SOFTWARE LIBRARY, VERSION 3.0 is an FDA 510(k)-cleared medical device (K062282) manufactured by Monebo Technologies, 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 March 21, 2007. Regulation: 8.