That seems to make more sense.  I don’t know anything about X-ray requirements 
but the FDA requirements laser interlocks are not specific, only referring to 
“interlocks”.
-Dave

From: MIKE SHERMAN [mailto:[email protected]]
Sent: Tuesday, February 05, 2019 12:27 PM
To: [email protected]
Subject: Re: [PSES] A question about FDA language and interlocking devices


Doug --



"knife-edge and finger stock" sounds more like the gasketing around the door to 
keep the radiation inside. I think you'll find similar gasketing on doors to 
EMC chambers. I've not heard of this term applied to interlock switches.



Mike Sherman

Graco Inc.


On February 5, 2019 at 10:35 AM Doug Nix <[email protected]<mailto:[email protected]>> 
wrote:

Colleagues,

I had a question come my way yesterday that I need a little help with. Here’s 
the question:

I have a customer that produces X-ray equipment. The FDA requires that the door 
that gives access to the X-ray source must have an interlock with a ‘knife-edge 
and finger stock’ type connection.  Also the FDA mentions that interlocks 
should be of conventional design. What is understood by “conventional design”?

My reading on this requirement is that any conventional electromechanical 
interlocking device like this:
[Image result for keyed interlock switch images]
will meet the basic requirements as described by the FDA as “knife-edge and 
fingerstock” connection, but I am concerned that this may not be at all what is 
meant.

As always, any guidance you can offer will be welcomed and appreciated!

Best,

Doug Nix
[email protected]<mailto:[email protected]>
+1 (519) 729-5704



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