K-number	K161559
Device name	Kuvia3D
Applicant	4qimaging, LLC Dba Qmetrics
Product code	LLZ
Device class	Class II
Decision date	Jun 23, 2016
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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Kuvia3D

Everything you need for a 510(k) submission. Nothing you don't.