K-number	K160558
Device name	RAPIDO HOLLOW-FIBRE DIALYZERS
Applicant	Bellco Srl
Product code	KDI
Device class	Class II
Decision date	Nov 18, 2016
Decision	Substantially Equivalent
Regulation	876.5860

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Source

View the full FDA submission: accessdata.fda.gov

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RAPIDO HOLLOW-FIBRE DIALYZERS

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