K-number	K233917
Device name	ICHOR 7F Embolectomy System (ICH-7F)
Applicant	Ichor
Product code	QEW
Device class	Class II
Decision date	Jul 18, 2024
Decision	Substantially Equivalent
Regulation	870.5150

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View the full FDA submission: accessdata.fda.gov

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ICHOR 7F Embolectomy System (ICH-7F)

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