K-number	K232417
Device name	MR Q; MR Q SUPINE; MR Q SLT
Applicant	Meridian AG
Product code	HQF
Device class	Class II
Decision date	Jan 25, 2024
Decision	Substantially Equivalent
Regulation	886.4390

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Source

View the full FDA submission: accessdata.fda.gov

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MR Q; MR Q SUPINE; MR Q SLT

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