K-number	K840527
Device name	COLOTRAK OCCULT BLOOD TEST
Applicant	Breit Laboratories, Inc.
Product code	KHE
Device class	Class II
Decision date	Sep 5, 1984
Decision	Substantially Equivalent
Regulation	864.6550

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View the full FDA submission: accessdata.fda.gov

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COLOTRAK OCCULT BLOOD TEST

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