K-number	K051114
Device name	SENTINEL AMMONIA ULTRA DIAGNOSTIC ASSAY
Applicant	Sentinel Ch. Srl
Product code	JIF
Device class	Class I
Decision date	Nov 25, 2005
Decision	Substantially Equivalent
Regulation	862.1065

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Source

View the full FDA submission: accessdata.fda.gov

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SENTINEL AMMONIA ULTRA DIAGNOSTIC ASSAY

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