K-number	K953239
Device name	BOEHRINGER MANNHEIM/HITACHI 917 ANALYZER
Applicant	Boehringer Mannheim Corp.
Product code	JJE
Device class	Class I
Decision date	Sep 25, 1995
Decision	Substantially Equivalent
Regulation	862.2160

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View the full FDA submission: accessdata.fda.gov

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BOEHRINGER MANNHEIM/HITACHI 917 ANALYZER

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