K-number	K231924
Device name	EZ-IO Intraosseous Vascular Access System
Applicant	Teleflex Medical
Product code	FMI
Device class	Class II
Decision date	Jul 25, 2023
Decision	Substantially Equivalent
Regulation	880.5570

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Source

View the full FDA submission: accessdata.fda.gov

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EZ-IO Intraosseous Vascular Access System

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