With regards to EN-60825, I would tend to believe (I did not want to say
'assume') that the
enforcement parallels the that for CE marking - customs, market
surveillance, customer/competitor
complaints, etc. 

In the US I would say it's 'the Feds'  -  21CFR 1040 is a 'Code of Federal
Regulations'. In this
case it would be agents from the FDA. But taking Doug McKean's response into
consideration,
focusing on OFCS, we can also include NRTLs in enforcement of compliance -
at least with
respect to the 'initial' compliance of the product. 

In the ITE standards (950, 1950, 60950) section 4.3.12 references lasers,
and notes that
equipment "shall be so designed that harmful effects to persons and
materials affecting
safety are prevented " . . .or something of that sort. In this case the NRTL
(at least the
big one that I use) would want to verify this - using 21CFR 1040 and EN
60825 as
their guide. I have had to provide not only the 'document received' letter
with accession
number from the CDRH, but also with the report that I filed. My listing was
contingent upon providing that supporting info. If you going to incorporate,
and not
modify an already classified laser, you would have submit that component
manufacturer's
supporting data.

While perhaps a definitive enforcement 'Agency X' does not exist, there are
hurdles that
need to be cleared. And considering today's economy, I wouldn't think any of
our employers would want to have trouble with 'the Feds'.

Just my own opinions . . . .

John Juhasz
Fiber Options
Div. of GE Interlogix
Bohemia, NY

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