K-number	K230372
Device name	VitreJect Syringe
Applicant	Ocuject, LLC
Product code	QLY
Device class	Class II
Decision date	Sep 8, 2023
Decision	Substantially Equivalent
Regulation	880.5860

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Source

View the full FDA submission: accessdata.fda.gov

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VitreJect Syringe

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