K-number	K100817
Device name	BIOSIGN IFOBTEST, BIOSIGN FECAL OCCULT BLOOD TEST
Applicant	Princeton BioMeditech Corp.
Product code	KHE
Device class	Class II
Decision date	Jul 1, 2010
Decision	Substantially Equivalent
Regulation	864.6550

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View the full FDA submission: accessdata.fda.gov

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BIOSIGN IFOBTEST, BIOSIGN FECAL OCCULT BLOOD TEST

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