K-number	K852086
Device name	CAPIOX BLOOD SAMPLING MANIFOLD
Applicant	Terumo Medical Corp.
Product code	DTL
Device class	Class II
Decision date	Aug 9, 1985
Decision	Substantially Equivalent
Regulation	870.4290

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View the full FDA submission: accessdata.fda.gov

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CAPIOX BLOOD SAMPLING MANIFOLD

Everything you need for a 510(k) submission. Nothing you don't.