K-number	K151709
Device name	Hi-Light Diagnostic Ultrasound Systems
Applicant	Qingdao Hisense Medical Equipment Co., Ltd.
Product code	IYO
Device class	Class II
Decision date	Jul 17, 2015
Decision	Substantially Equivalent
Regulation	892.1560

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View the full FDA submission: accessdata.fda.gov

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Hi-Light Diagnostic Ultrasound Systems

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