K-number	K230743
Device name	ICHOR 14F Embolectomy System
Applicant	Ichor
Product code	QEW
Device class	Class II
Decision date	Sep 5, 2023
Decision	Substantially Equivalent
Regulation	870.5150

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Source

View the full FDA submission: accessdata.fda.gov

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ICHOR 14F Embolectomy System

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