K-number	K981480
Device name	PHILIPS EASYGUIDE
Applicant	Philips Medical Systems, Inc.
Product code	HAW
Device class	Class II
Decision date	Jan 28, 1999
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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PHILIPS EASYGUIDE

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