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FDA regulations A
U.S. Food and Drug Administration (FDA) has implemented regulations for laser products
manufactured on and after August 2, 1976. Compliance is mandatory for products marketed in the
United States. The following label on the back of the machine indicates compliance with the FDA
regulations and must be attached to laser products marketed in the United States.
WARNING
Use of controls, adjustments or performance of procedures other than those specified in this
manual may result in hazardous invisible radiation exposure.
Internal laser radiation
Max. Radiation Power 5 mW
Wave Length 770 – 810 nm
Laser Class Class 3B
Manufactured:
BROTHER TECHNOLOGY (SHENZHEN) LTD.
NO6 Gold Garden Ind. Nanling Buji, Longgang, Shenzhen, China.
This product complies with FDA performance standards for laser products except for deviations
pursuant to Laser Notice No. 50, dated July 26, 2001.