K-number	K042540
Device name	PHILIPS IU22 ULTRASOUND SYSTEM
Applicant	Philips Ultrasound, Inc.
Product code	IYO
Device class	Class II
Decision date	Oct 4, 2004
Decision	Substantially Equivalent
Regulation	892.1560

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View the full FDA submission: accessdata.fda.gov

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PHILIPS IU22 ULTRASOUND SYSTEM

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