K-number	K230959
Device name	VitreJect® Needle; OcuSafe® Needle
Applicant	Ocuject, LLC
Product code	FMI
Device class	Class II
Decision date	Sep 14, 2023
Decision	Substantially Equivalent
Regulation	880.5570

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Source

View the full FDA submission: accessdata.fda.gov

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VitreJect® Needle; OcuSafe® Needle

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