K-number	K222395
Device name	Tango Neo, Tango Reflex Neo, Ultra Q Reflex Neo
Applicant	Ellex Medical Pty, Ltd.
Product code	HQF
Device class	Class II
Decision date	Nov 2, 2022
Decision	Substantially Equivalent
Regulation	886.4390

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View the full FDA submission: accessdata.fda.gov

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Tango Neo, Tango Reflex Neo, Ultra Q Reflex Neo

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