K-number	K182302
Device name	CardioGard Emboli Protection Cannula
Applicant	Cardiogard Medical, Ltd.
Product code	DWF
Device class	Class II
Decision date	May 17, 2019
Decision	Substantially Equivalent
Regulation	870.4210

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Source

View the full FDA submission: accessdata.fda.gov

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CardioGard Emboli Protection Cannula

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