K-number	K130499
Device name	IU22 DIAGNOSTIC ULTRASOUND SYSTEM
Applicant	Philips Ultrasound, Inc.
Product code	IYN
Device class	Class II
Decision date	Jun 18, 2013
Decision	Substantially Equivalent
Regulation	892.1550

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Source

View the full FDA submission: accessdata.fda.gov

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IU22 DIAGNOSTIC ULTRASOUND SYSTEM

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