K-number	K812604
Device name	BIOVATION URINALYSIS REPORTER
Applicant	Biovation, Inc.
Product code	JQP
Device class	Class I
Decision date	Oct 2, 1981
Decision	Substantially Equivalent
Regulation	862.2100

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View the full FDA submission: accessdata.fda.gov

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BIOVATION URINALYSIS REPORTER

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