K-number	K030734
Device name	PATHWAY ACCESS SHEATH CATHETER
Applicant	Vertelink Corporation
Product code	DYB
Device class	Class II
Decision date	Sep 10, 2003
Decision	Substantially Equivalent
Regulation	870.1340

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Source

View the full FDA submission: accessdata.fda.gov

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PATHWAY ACCESS SHEATH CATHETER

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