K-number	K926359
Device name	CLINITEK 200+ URINE CHEMISTRY ANALYZER
Applicant	Heraeus Kulzer, Inc.
Product code	KQO
Device class	Class I
Decision date	Jan 28, 1993
Decision	Substantially Equivalent
Regulation	862.2900

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View the full FDA submission: accessdata.fda.gov

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CLINITEK 200+ URINE CHEMISTRY ANALYZER

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