K-number	K945705
Device name	5F ENVOY(TM) GUIDING CATHETER
Applicant	Cordis Neurovascular, Inc.
Product code	DQY
Device class	Class II
Decision date	Feb 3, 1995
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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5F ENVOY(TM) GUIDING CATHETER

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