240 Technical Specifications
CDRH regulations
The Center for Devices and Radiological Health (CDRH) of the
U.S. Food and Drug Administration implemented regulations for
laser products on August 2, 1976. Compliance is mandatory for
products marketed in the United States. The label shown below
indicates compliance with the CDRH regulations and must be
attached to laser products marketed in the United States.
Interfaces
Parallel interface
Use an IEEE 1284-I compliant parallel interface connector.
ECP mode/Nibble mode
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