K-number	K182274
Device name	Orbit Subretinal Delivery System
Applicant	Orbit Biomedical, Inc.
Product code	FMF
Device class	Class II
Decision date	Nov 20, 2018
Decision	Unknown
Regulation	880.5860

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Source

View the full FDA submission: accessdata.fda.gov

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Orbit Subretinal Delivery System

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