Fda Regulations - Brother MFC-8440 User Manual

Since radiation emitted inside the equipment is completely confined
within protective housings and external covers, the laser beam
cannot escape from the MFC during any phase of user operation.

FDA regulations

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 MFC indicates
compliance with the FDA regulations and must be attached to laser
products marketed in the United States.
Manufactured:
BROTHER CORP. (ASIA) LTD.
BROTHER BUJI NAN LING FACTORY
Gold Garden Industry, Nan Ling Village, Buji, Rong Gang,
Shenzhen, China.
This product complies with FDA radiation performance standards,
21 CFR Subchapter J.
WARNING
Use of controls, adjustments or performance of procedures other
than those specified in this manual may result in hazardous invisible
radiation exposure.
WARNING
Changes or modifications not expressly approved by Brother
Industries, Ltd. may void the user's authority to operate the
equipment.
Internal laser radiation
Max. Radiation Power
Wave Length
Laser Class
21 - 5 IMPORTANT INFORMATION
5 mW
760 - 810 nm
Class IIIb (Accordance with 21 CFR
Part 1040.10)