FDA
Export to US
The laser product mounted on equipment and exported to the United States is
subjected to the regulation of the Food and Drug Administration (FDA). In order to
prevent the users' injury caused by laser products, the FDA specifies PART 1040
(Performance Standards for Light-Emitting Products). The FDA classifies laser
products according to the degree of risk and provides safety measures for
respective classes. (
● Certification and Identification Label
<Label position>
Ramco National
refer to "FDA Standards".)
800-280-6933 | nsales@ramcoi.com
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