K-number	K231709
Device name	AcuityDR 1013 G4, AcuityDR 1417 G4, AcuityDR 1717G4
Applicant	Radmedix, LLC
Product code	MQB
Device class	Class II
Decision date	Jul 12, 2023
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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AcuityDR 1013 G4, AcuityDR 1417 G4, AcuityDR 1717G4

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