Fluke-biomedical 451P User Manual download pdf (Page 4)

To ensure the accuracy of the Product is maintained at a high level, Fluke Biomedical recommends the product

be calibrated at least once every 12 months. Calibration must be done by qualified personnel. Contact your local

Fluke Biomedical representative for calibration.

Certification

This instrument was thoroughly tested and inspected. It was found to meet Fluke Biomedical’s manufacturing

specifications when it was shipped from the factory. Calibration measurements are traceable to the National Institute of

Standards and Technology (NIST). Devices for which there are no NIST calibration standards are measured against in-

house performance standards using accepted test procedures.

WARNING

Unauthorized user modifications or application beyond the published specifications may result in electrical shock hazards

or improper operation. Fluke Biomedical will not be responsible for any injuries sustained due to unauthorized equipment

modifications.

Restrictions and Liabilities

Information in this document is subject to change and does not represent a commitment by Fluke Biomedical.

Changes made to the information in this document will be incorporated in new editions of the publication. No

responsibility is assumed by Fluke Biomedical for the use or reliability of software or equipment that is not

supplied by Fluke Biomedical, or by its affiliated dealers.

Manufacturing Location

The 451P Ion Chamber Survey Meter is manufactured at Fluke Biomedical, 6920 Seaway Blvd., Everett, WA,

U.S.A.

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Fluke-biomedical 451P User Manual Page 4