K-number	K051526
Device name	URITEK-720+ URINE ANALYZER
Applicant	Teco Diagnostics
Product code	KQO
Device class	Class I
Decision date	Aug 16, 2005
Decision	Substantially Equivalent
Regulation	862.2900

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Source

View the full FDA submission: accessdata.fda.gov

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URITEK-720+ URINE ANALYZER

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