K-number	K170574
Device name	Diacap Pro Dialyzer
Applicant	B. Braun Avitum AG
Product code	KDI
Device class	Class II
Decision date	Aug 11, 2017
Decision	Substantially Equivalent
Regulation	876.5860

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Source

View the full FDA submission: accessdata.fda.gov

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Diacap Pro Dialyzer

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