BEES 2.0

This group is here to discuss all matters pertaining to the BEES upgrade project.

Device users and distributors have to submit info about the pati

Extensive and ongoing training in how to use and interpret data is regulated. If I were to ask you, "Who is the buyer of your medical devices. The question pertains to approval in Europe, Australia, Japan, Canada and how that relates to a US approval, and secondly, what type of 510(k) to prepare in the US.  My blog  http://www.videomakerfxdownload.com/
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Wednesday, September 14, 2016
 
 

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