K-number	K152899
Device name	Philips Lumify Diagnostic Ultrasound System
Applicant	Philips Healthcare, Inc.
Product code	IYN
Device class	Class II
Decision date	Oct 30, 2015
Decision	Substantially Equivalent
Regulation	892.1550

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Source

View the full FDA submission: accessdata.fda.gov

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Philips Lumify Diagnostic Ultrasound System

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