- ECG data is necessary for the diagnosis of all cardiac arrhythmias in order to assess severity, implications and treatment options.
- HeartBeam is reporting that its 12-lead ECG synthesis software for arrhythmia assessment has been submitted to the U.S. Food and Drug Administration for 510(k) clearance.
- To enable smooth commercialization, the company is building the infrastructure needed to support widespread adoption.
In the world of heart health, palpitations are common, with atrial fibrillation (“AF”) being one of the most typical sustained arrhythmias in adults (https://ibn.fm/8TSNY). HeartBeam (NASDAQ: BEAT) is on the verge of transforming how AF is detected and managed with its breakthrough, cable-free ECG technology (https://ibn.fm/B16MX).
“Most palpitations occur during normal sinus rhythm, and AF can be the cause of palpitations,” states a Journal of Internal Medicine report. “However, it is often asymptomatic. In contrast to the majority of palpitations which are benign in nature, AF is associated with increased risk for…
NOTE TO INVESTORS: The latest news and updates relating to BEAT are available in the company’s newsroom at https://ibn.fm/BEAT
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