Preventice received 510(k) clearance from the U.S. Food and Drug Administration (FDA) in August, enabling the mobile health solutions company to market and sell BodyGuardian to hospitals and clinics for use in detecting and monitoring non-lethal cardiac arrhythmias for ambulatory patients.About BodyGuardian
Preventice Progresses Toward Commercial Availability Of Its BodyGuardian Remote Patient Monitoring System™
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