K-number	K901887
Device name	MODIFIED SEPACELL R-SERIES BLOOD FILTERS
Applicant	Asahi Medical Co., Ltd.
Product code	CAK
Device class	Class II
Decision date	Aug 8, 1990
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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MODIFIED SEPACELL R-SERIES BLOOD FILTERS

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