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Pathway Genomics Corporation Obtains FDA Registration


9/28/2011 8:49:37 AM

SAN DIEGO--(BUSINESS WIRE)--The U.S. Food and Drug Administration (FDA) has classified and registered Pathway Genomics’ proprietary saliva collection kit as a Class I exempt device. With guidance from licensed health care providers, Pathway’s saliva collection kit is used to collect samples from patients for genetic testing purposes.

Read at BioSpace.com

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