K-number	K063673
Device name	INNOVACON FLIPCARD FECAL OCCULT BLOOD TEST DEVICE
Applicant	Innovacon, Inc.
Product code	KHE
Device class	Class II
Decision date	Mar 5, 2007
Decision	Substantially Equivalent
Regulation	864.6550

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View the full FDA submission: accessdata.fda.gov

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INNOVACON FLIPCARD FECAL OCCULT BLOOD TEST DEVICE

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