K-number	K002026
Device name	CAPIOX ARTERIAL FILTER
Applicant	Terumo Medical Corp.
Product code	DTM
Device class	Class II
Decision date	Sep 6, 2000
Decision	Substantially Equivalent
Regulation	870.4260

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Source

View the full FDA submission: accessdata.fda.gov

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CAPIOX ARTERIAL FILTER

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