K-number	K923139
Device name	HEMOCOR HP HEMOCONCENTRATOR SERIES
Applicant	Minntech Corp.
Product code	KDI
Device class	Class II
Decision date	Feb 18, 1994
Decision	Substantially Equivalent
Regulation	876.5860

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View the full FDA submission: accessdata.fda.gov

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HEMOCOR HP HEMOCONCENTRATOR SERIES

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