IASIS Neurofeedback treats the source - not the symptoms; by helping the brain and central nervous system to get reorganized.
IASIS Neurofeedback treats the source - not the symptoms; by helping the brain and central nervous system to get reorganized.
IASIS is a safe technology that uses brainwave feedback (EEG) to help the brain reboot itself.
Caused by stress, illness, traumatic injuries, environmental factors, etc., brainwaves can become stuck in patterns that become brain related disorders. IASIS helps to disrupt the patterns and bring the brain and central nervous system back into balance, forming new, healthier brain wave patterns.
The IASIS Neurofeedback device is indicated for relaxation training and muscle reeducation and prescription use consistent with 21 C.F.R. section 882.5050.
The ease and simplicity of treatment all distinguish it from a traditional neurofeedback device.
IASIS Neurofeedback is imperceptible and non-invasive and effortless to the client.
Perinatal Mood/Anxiety Disorders
Traumatic Birth
Overstimulated Baby
ADD/ADHD
Food Aversions
Addictions
Anxiety
Chronic Fatigue Syndrome
Depression
Fibromyalgia
Headache/Migraine
Insomnia
Memory Disorders
PTSD
We love our fur friends, and we want them to experience their best life. If your pet is irritable, stressed, anxious or in chronic pain; help is available for them too!
is an IASIS Microcurrent Neurofeedback Certified Provider, serving all of San Diego county. She works with all ages from infant to adult, as well as large animals including horses and dogs. Home visits are available upon request.
2667 Camino del Rio S, Suite 201, San Diego, California 92108, United States
PART 882 -- NEUROLOGICAL DEVICES
Subpart F - Neurological Therapeutic Devices
Sec. 882.5050 Biofeedback device.
(a) Identification. A biofeedback device is an instrument that provides a visual or auditory signal corresponding to the status of one or more of a patient's physiological parameters (e.g., brain alpha wave activity, muscle activity, skin temperature, etc.) so that the patient can control voluntarily these physiological parameters.
(b) Classification. Class II (special controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter when it is a prescription battery powered device that is indicated for relaxation training and muscle reeducation and prescription use, subject to § 882.9.
[44 FR 51730, Sept. 4, 1979, as amended at 63 FR 59229, Nov. 3, 1998]
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