K-number	K150580
Device name	UltraVision 2 Diagnostic Ultrasound System
Applicant	Winprobe Corporation
Product code	IYO
Device class	Class II
Decision date	Apr 7, 2015
Decision	Substantially Equivalent
Regulation	892.1560

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View the full FDA submission: accessdata.fda.gov

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UltraVision 2 Diagnostic Ultrasound System

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