FDA regulations- Page 110

96

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.