K-number	K905782
Device name	FHT (FECAL HEME TEST)
Applicant	Aerscher, Inc.
Product code	KHE
Device class	Class II
Decision date	May 6, 1991
Decision	Substantially Equivalent
Regulation	864.6550

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View the full FDA submission: accessdata.fda.gov

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FHT (FECAL HEME TEST)

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