K-number	K182153
Device name	Ultrasound System SONIMAGE HS1
Applicant	Konica Minolta, Inc.
Product code	IYO
Device class	Class II
Decision date	Sep 6, 2018
Decision	Substantially Equivalent
Regulation	892.1560

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View the full FDA submission: accessdata.fda.gov

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Ultrasound System SONIMAGE HS1

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