K-number	K761148
Device name	REFLOMAT/REFLOTEST SYSTEM
Applicant	Boehringer Mannheim Corp.
Product code	CGA
Device class	Class II
Decision date	Feb 11, 1977
Decision	Substantially Equivalent
Regulation	862.1345

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View the full FDA submission: accessdata.fda.gov

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REFLOMAT/REFLOTEST SYSTEM

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