K-number	K942364
Device name	HITACHI 914 ANALYZER
Applicant	Boehringer Mannheim Corp.
Product code	JJE
Device class	Class I
Decision date	Oct 4, 1994
Decision	Substantially Equivalent
Regulation	862.2160

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View the full FDA submission: accessdata.fda.gov

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HITACHI 914 ANALYZER

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