K-number	K120489
Device name	TISSUE OF ORIGIN TEST KIT FFPE
Applicant	Pathwork Diagnostics, Inc.
Product code	OIW
Device class	Class II
Decision date	May 17, 2012
Decision	Substantially Equivalent
Regulation	862.3100

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Source

View the full FDA submission: accessdata.fda.gov

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TISSUE OF ORIGIN TEST KIT FFPE

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