TITLE

Pathway Genomics Obtains FDA Registration

PUB. DATE
September 2011
SOURCE
Biomedical Market Newsletter;9/30/2011, Vol. 21, p268
SOURCE TYPE
Periodical
DOC. TYPE
Article
ABSTRACT
The article reports on the classification and registration of Pathway Genomics Corp.'s proprietary saliva collection kit as a Class I exempt device approved by the U.S. Food & Drug Administration (FDA). It notes that the kit helps patients and physicians with an effective and safe method of providing samples for genetic testing purposes. It also states that under FDA's regulations, Class I exempt devices are manufactured under a specific quality assurance program.
ACCESSION #
69746810

 

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