K-number	K021422
Device name	PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02
Applicant	Philips Medical Systems
Product code	MHX
Device class	Class II
Decision date	May 15, 2002
Decision	Substantially Equivalent
Regulation	870.1025

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View the full FDA submission: accessdata.fda.gov

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PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02

Everything you need for a 510(k) submission. Nothing you don't.