K-number	K882895
Device name	MODIFIED BETA QUIK STAT EIA KIT
Applicant	Pacific Biotech, Inc.
Product code	DHA
Device class	Class II
Decision date	Oct 12, 1988
Decision	Substantially Equivalent
Regulation	862.1155

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View the full FDA submission: accessdata.fda.gov

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MODIFIED BETA QUIK STAT EIA KIT

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