K-number	K230819
Device name	OmniGuide RFID Surgical Laser Fibers
Applicant	Omni-Guide Holdings, Inc.
Product code	GEX
Device class	Class II
Decision date	Apr 21, 2023
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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OmniGuide RFID Surgical Laser Fibers

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