K-number	K022788
Device name	PHILIPS HARMONY RELEASE 1
Applicant	Philips Medical Systems North America Co.
Product code	LLZ
Device class	Class II
Decision date	Oct 25, 2002
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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PHILIPS HARMONY RELEASE 1

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