K-number	K960546
Device name	CLINITEK 50 URINE CHEMISTRY ANALYZER
Applicant	Bayer Corp.
Product code	KQO
Device class	Class I
Decision date	Jun 12, 1996
Decision	Substantially Equivalent
Regulation	862.2900

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View the full FDA submission: accessdata.fda.gov

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CLINITEK 50 URINE CHEMISTRY ANALYZER

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