K-number	K223125
Device name	XR90 (XR90-SYS)
Applicant	Mediview Xr, Inc.
Product code	LLZ
Device class	Class II
Decision date	Jul 13, 2023
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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XR90 (XR90-SYS)

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