Specification
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EMC – Information
Declaration of Conformity with USA Federal Communications
Commission (FCC) and Canadian Ministry of Health Rules for
Electromagnetic Compatibility
The Nox T3 device complies with Part 15 of the FCC Rules and RSS 210 of Industry Canada.
Operation is subject to the following two conditions:
1.
This device may not cause harmful interference, and
2.
This device must accept any interference, including interference that may cause undesired
operation of this device.
For questions regarding your product or this FCC declaration, please contact:
Fusion Sleep Therapy Services LLC
4265 Johns Creek Parkway, suite A
Suwanee
GA 30024
USA
Phone: 678 990 3262
Fax: 678 990 3966
Email: [email protected]
This equipment has been tested and found to comply with the limits for a Class B digital device,
pursuant to Part 15 of FCC Rules. These limits are designed to provide reasonable protection against
harmful interference in a residential installation. This equipment generates, uses, and can radiate radio
frequency energy. If not installed and used in accordance with the instructions, it may cause harmful
interference to radio communications. However, there is no guarantee that interference will not occur in
a particular installation.
If this equipment does cause harmful interference to radio or television reception, which can be
determined by tuning the equipment off and on, the user is encouraged to try and correct the
interference by one or more of the following measures:
•
Reorient or relocate the receiving antenna.
•
Increase the distance between the equipment and the receiver.
•
Connect the equipment to outlet on a circuit different from that to which the receiver is
connected.
•
Consult the dealer or an experienced radio/TV technician for help.
Modification Statement
The FCC requires the user to be notified that any changes or modifications not expressly approved by
Nox Medical could void the user's authority to operate the equipment.
