K-number	K984269
Device name	DBEST OCCULT BLOOD TEST KIT
Applicant	Ameritek, Inc.
Product code	KHE
Device class	Class II
Decision date	May 11, 1999
Decision	Substantially Equivalent
Regulation	864.6550

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Source

View the full FDA submission: accessdata.fda.gov

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DBEST OCCULT BLOOD TEST KIT

Everything you need for a 510(k) submission. Nothing you don't.