Fluke Biomedical 601PRO XL - Manual (Page 8)

6 0 1 P R O S E R I E S
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Electromagnetic Interference and Susceptibility
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USA FCC CLASS A
Warning: Changes or modifications to this unit not expressly approved by the
manufacturer could void the user's authority to operate the equipment.
This equipment has been tested and found to comply with the limits for a Class A digital
device, pursuant to Part 15 of the FCC Rules.
These limits are designed to provide reasonable protection against harmful interference
when the equipment is operated in a commercial environment. Like all similar equipment,
this equipment generates, uses, and can radiate radio frequency energy and, if not installed
and used in accordance with the instruction manual, may cause harmful interference to
radio communications. Operation of this equipment in a residential area is likely to cause
interference, in which case the user will be required to correct the interference at his own
expense.
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Canadian Department of Communications Class A
This digital apparatus does not exceed Class A limits for radio emissions from digital
apparatus set out in the Radio Interference Regulations of the Canadian Department of
Communications.
Le present appareil numerique n'met pas du bruits radioelectriques depassant les limites
applicables aux appareils numerique de la Class A prescrites dans le Reglement sur le
brouillage radioelectrique edicte par le ministere des Communications du Canada.
User Safety
This device has been type tested by an independent laboratory and found to meet the
requirements of the following:
Canadian Standards Association CAN/CSA
C22.2 No.1010.1-1992, “Safety Requirements for Electrical Equipment for
Measurement, Control and Laboratory Use, Part 1: General Requirements”.
UL 3101-1
“Electrical Equipment for Laboratory Use, Part 1: General Requirements”.