K-number	K771206
Device name	AV FISTULA NEEDLE SET
Applicant	Terumo America, Inc.
Product code	FIE
Device class	Class II
Decision date	Jul 15, 1977
Decision	Substantially Equivalent
Regulation	876.5540

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View the full FDA submission: accessdata.fda.gov

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AV FISTULA NEEDLE SET

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