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Airstrip Technologies, LP
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AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING SOFTWARE, VERSION 3.1 is an FDA 510(k)-cleared medical device (K100133) manufactured by Airstrip Technologies, LP. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 22, 2010. Regulation: 8.