K-number	K993634
Device name	CARESIDE ANALYZER
Applicant	Careside, Inc.
Product code	JJF
Device class	Class I
Decision date	Dec 2, 1999
Decision	Substantially Equivalent
Regulation	862.2170

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Source

View the full FDA submission: accessdata.fda.gov

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CARESIDE ANALYZER

Everything you need for a 510(k) submission. Nothing you don't.