FW Fisher Wallace Stimulator Instruction Manual

THE FISHER WALLACE STIMULATOR FOR THE TREATMENT OF PAIN ON THE BODY
INSTRUCTION MANUAL. Call us with any questions: (800) 692 - 4380

1.0 INTRODUCTION

The Fisher Wallace Stimulator is a portable, battery-powered device which has been cleared by the FDA for
symptomatic relief of chronic pain, post-traumatic acute pain and post-surgical pain when used on the body. The
device is also cleared by the FDA for the treatment of depression, anxiety and insomnia. Although the device
poses no significant risks to health, patients should be monitored by their physician at least once every three
months while using the device; more frequent monitoring is recommended. Do not attempt to reduce or cease
use of other medication without first consulting your doctor.
The device delivers a micro-electrical stimulus (1-4 mA) that is carried by electrical cables to wet sponges (supplied
with the device) that are applied to the skin. When treating site-specific pain on the body, the electrodes are
placed on the body. As clearly illustrated in this manual on pages 6-12, the red wire electrode is typically placed at
the rear base of the neck and the black wire electrode is placed on the pain site (with the exception of gastro pain
treatment). The electrodes are secured to the body with Velcro body straps, which are included in the kit.
Read section 10.0 APPLICATION OF THE DEVICE ON THE BODY for instructions for use, as well
as the Treatment Diagrams on pages 6-12 for guidance regarding the treatment of Back Pain, Shoulder
Pain, Gastro Pain, Elbow Pain, Phantom Limb Pain, Arthritic Pain and Neck Pain.
Please email us at info@fisherwallace.com or call us at (800) 692 - 4380 with any questions.

2.0 CONTRAINDICATIONS

The device is contraindicated for use in patients who have demand or sensing type cardiac pacemakers.
3.0 WARNINGS
Keep the device out of the reach of children. Electronic monitoring equipment (such as ECG monitors, ECG
alarms) may not operate properly when CES stimulation is in use. High Frequency surgical equipment may not be
used when CES stimulation is in use. Do not operate the CES stimulator in close proximity to short-wave or
microwave therapy equipment.
This device is not suitable for use with oxygen or in the presence of a flammable anesthetic mixture with air or
oxygen, or with nitrous oxide.

4.0 PRECAUTIONS

This device should not be used on the throat or neck, except the rear base of the neck as indicated in the diagrams
for treating pain (see the Chronic Pain Instruction Manual). This device should not be used on the eyes. This
device should not be used on or near areas of the body, including the head, that contain implanted devices, such as
stimulators, stents, and active or inactive implants such as deep brain stimulators and vagus nerve stimulators.
Patients should avoid using the device near areas of the body where there is embedded shrapnel or metal plates.
There is no danger in using the device if you have dental fillings.
Do not allow water to enter this device. The Fisher Wallace Stimulator should not be exposed to environmental
conditions where the system may get wet.
5.0 ADVERSE REACTIONS (VERY RARE)
Skin irritation may occur at the site of sponge electrode placement, especially if the sponges deteriorate (sponges
should be replaced EVERY TWO WEEKS) or if contact is made between the skin and the metal part of the
sponge receptacle, or if the sponges are not thoroughly wet before each use. A mild headache or dizziness may
occur, and should cease after you stop using the device. Such reactions are very rare.
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