AliveCor receives FDA clearance on its mobile heart monitor

Published on December 3, 2012 at 9:33 AM · No Comments

AliveCor, Inc. announced today at the start of the 4th annual mHealth Summit in Washington, D.C. that the company received FDA 510(k) clearance on its mobile Heart Monitor as well as CE Mark conformity. This clinical-quality, low-cost mobile ECG heart monitor, compatible with the iPhone® 4 and 4S, enables doctors to evaluate patient heart health easily, quickly and remotely.

“Our goal is to make health care cheaper, easier and more readily available without losing quality of care”

Clinical studies of the device indicate that a high-quality single-channel ECG can be rapidly and simply recorded using an iPhone with the AliveCor application and device, to accurately screen for cardiac arrhythmias including atrial fibrillation. Atrial fibrillation is the most commonly occurring arrhythmia and carries a five-fold increased risk of stroke.

Additionally, AliveCor's founder, Dr. David Albert, and co-founders Bruce Satchwell and Kim Barnett were granted U.S. Patent No. 8,301,232 for the device and technology. The three colleagues began working on the heart-monitoring device in 2008.

"We believe that mobile ECGs and other breakthroughs in mobile health can significantly change the way medicine is delivered," Dr. Albert said.

AliveCor's Heart Monitor is initially intended for use by licensed medical professionals to record, display, store, transfer, and evaluate single-channel electrocardiogram (ECG) rhythms.

The rhythm strips can be of any duration, and are stored on the iPhone and securely in the cloud for later analysis, sharing and printing through AliveCor's secure website. The ECG data is sent wirelessly from the Heart Monitor via AliveCor's low-power, proprietary communication protocol, and requires no pairing between the iPhone and the device.

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