K-number	K013013
Device name	MEDTRONIC DLP ARTERIAL CANNULA WITH 3D TIP - 22 FR.
Applicant	Medtronic Cardiac Surgical Products
Product code	DWF
Device class	Class II
Decision date	Dec 4, 2001
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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MEDTRONIC DLP ARTERIAL CANNULA WITH 3D TIP - 22 FR.

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