K-number	K781954
Device name	CATHETER INTRODUCERS, ARTERISE
Applicant	C.R. Bard, Inc.
Product code	DYB
Device class	Class II
Decision date	Nov 29, 1978
Decision	Substantially Equivalent
Regulation	870.1340

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View the full FDA submission: accessdata.fda.gov

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CATHETER INTRODUCERS, ARTERISE

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