K-number	K123762
Device name	DLP RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH AUTO-INFLATE CUFF
Applicant	Medtronic, Inc.
Product code	DWF
Device class	Class II
Decision date	Mar 27, 2013
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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DLP RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH AUTO-INFLATE CUFF

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