K-number	K934533
Device name	BUN-300/BUN-500 UREA NITROGEN REAGENT
Applicant	Horizon Diagnostics, Inc.
Product code	CDQ
Device class	Class II
Decision date	Nov 26, 1993
Decision	Substantially Equivalent
Regulation	862.1770

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View the full FDA submission: accessdata.fda.gov

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BUN-300/BUN-500 UREA NITROGEN REAGENT

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