K-number	K162585
Device name	SuniIQ Digital Radiography System
Applicant	Suni Medical Imaging, Inc.
Product code	MUH
Device class	Class II
Decision date	Nov 4, 2016
Decision	Substantially Equivalent
Regulation	872.1800

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Source

View the full FDA submission: accessdata.fda.gov

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SuniIQ Digital Radiography System

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