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RESPeRATE Ultra - Blood Pressure Lowering Device For Non-Drug Hypertension Reduction
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RESPeRATE Ultra - Blood Pressure Lowering Device Features
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LOWER BLOOD PRESSURE NATURALLY: RESPeRATE is an FDA-cleared, non-drug medical device clinically proven to reduce blood pressure. It offers all-day sustained BP reduction in 3-4 weeks of use and its only reported “side effect” is better sleep.
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CLINICALLY PROVEN, DOCTOR-RECOMMENDED HEART HEALTH SUPPORT: RESPeRATE’s safety and efficacy in lowering blood pressure were demonstrated repeatedly in 19 separate clinical research studies published in peer-reviewed medical journals on hypertension.
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PATENTED TECHNOLOGY: RESPeRATE’s sensor picks up the breathing movements and turns them into tones that gradually prolong exhalation and slow breathing. Each prolonged exhalation relaxes constricted blood vessels, reducing blood pressure naturally.
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JUST 15 MINUTES A DAY: Breathe with the guiding tones 15 minutes a day, 3-4 times a week. As the effect accumulates, constricted blood vessels relax, leading to lasting, all-day blood pressure reduction in a few weeks.
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100% COMMITTED TO LOWERING BLOOD PRESSURE: RESPeRATE product specialists are available by phone for technical or any other issue. RESPeRATE has a 1-year warranty, is available without a prescription, and is eligible for FSA and HSA reimbursement plans.
About RESPeRATE Ultra - Blood Pressure Lowering Device
RESPeRATE is the only FDA-cleared, non-drug, non-invasive device for hypertension Treatment. Used by over 250,000 patients and physicians, it is recommended by the American Heart Association (AHA) scientific statement on non-pharmacological treatments for Lowering High Blood Pressure. The RESPeRATE device lowers blood pressure by relaxing constricted blood vessels which cause high blood pressure. RESPeRATE does so by harnessing the therapeutic power of slow paced breathing with prolonged exhalation in a way that is virtually impossible to achieve on your own. All you have to do is breathe along with RESPeRATE’s guiding tones. FDA clearance #K020399 (OTC).
