Josh - For clarification, the FDA requirements do not apply Laser Class I sources or products, since a warning logotype or warning statement is not required.
You're right that IEC 60825-1 requires only laser class be identified in all literature, but even so, for laser products only, implying it's not necessary for laser sources. Probably a good idea to include this information in all cases (classes, devices, sources and products) since Class I/1 is desirable and is shopped for in many applications, and it allows compliance in a more globally for the remainder. But it's not always a required for compliance purposes. Regards, Peter L. Tarver, PE [email protected] > -----Original Message----- > From: Josh Wiseman > Sent: Wednesday, June 08, 2005 6:04 AM > > > Mac, > > The only requirement for this kind of info that I > recall is for Laser > Devices. The Laser Class must be called out on > all literature. > > Regards, > Josh > This message is from the IEEE Product Safety Engineering Society emc-pstc discussion list. Website: http://www.ieee-pses.org/ To post a message to the list, send your e-mail to [email protected] Instructions: http://listserv.ieee.org/listserv/request/user-guide.html List rules: http://www.ieee-pses.org/listrules.html For help, send mail to the list administrators: Scott Douglas [email protected] Mike Cantwell [email protected] For policy questions, send mail to: Richard Nute: [email protected] Jim Bacher: [email protected] All emc-pstc postings are archived and searchable on the web at: http://www.ieeecommunities.org/emc-pstc
