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®
NEUROPROBE
500 PRO USER MANUAL
SLD INFRARED PADS:
Wavelengths:
Diodes and Dimensions:
TIMER FUNCTIONS:
Treatment Timer:
PROBE DETECTION:
Sensitivity:
Display:
Audio:
PATIENT SAFETY SYSTEMS:
Activation:
MISC:
Auto Intensity:
Treatment Programs:
Certificates and Approvals:
Caution:
NOTE: ACP reserves the right to change technical specifications and product availability without notice.
COPYRIGHT © 2006 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
SPECIFICATIONS (Cont.)
630nm with 875 nm
15 x 630nm & 24 x 875nm on each 4.5" x 7.5" pad in dual pad configuration
110 x 630 nm and 48x875 nm on a 29" x 14" L.E. Pad
Adjustable for 1-99 minutes in one-minute increments in IFC modes. In probe mode the time is
adjustable from 1-999 seconds. Tums output to zero and system off and sounds 10-second
buzzer to indicate completion of treatment in IFC modes. In probe mode the system returns to
the detection mode following time out.
Adjustable from 200K to 5 Meg ohms
Bar graph and numeric indicator 0-200uA
Variable frequency increases with skin conductivity
By patient safety hand control which shuts down output. Output modality may not be changed
during operation. Output levels are reset to zero at the start and completion of treatment.
Output intensity is gradually increased during treatment from 0 to 20% automatically in a linear manner
over the duration of treatment when the anti-adaptation mode is selected. The amount of increase is user
programmable.
Infrared Therapy: 1 Preset
Sensory-Motor: 7 Presets
Noxious: 1 Preset
Nerve Block: 2 Presets
For program details see Page 24
Device is designed to meet or exceed all safety requirements of a medical device in it's class, per
IEC 60601 and CSA C22.2 No. 601.1
Federal law restricts this device to sale by or on the order of a physician (or other health
practitioner licensed by their state).
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