K-number	K202216
Device name	EPIQ Series Diagnostic Ultrasound Systems
Applicant	Philips Ultrasound, Inc.
Product code	IYN
Device class	Class II
Decision date	Sep 2, 2020
Decision	Substantially Equivalent
Regulation	892.1550

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Source

View the full FDA submission: accessdata.fda.gov

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EPIQ Series Diagnostic Ultrasound Systems

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