K-number	K801632
Device name	THE BELLCO FISTULA NEEDLES
Applicant	Bellco Artifidial Organ Spec., Inc.
Product code	FIE
Device class	Class II
Decision date	Aug 4, 1980
Decision	Substantially Equivalent
Regulation	876.5540

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View the full FDA submission: accessdata.fda.gov

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THE BELLCO FISTULA NEEDLES

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