K-number	K042671
Device name	PLANMED SOPHIE NUANCE CLASSIC
Applicant	Planmed OY
Product code	IZH
Device class	Class II
Decision date	Nov 19, 2004
Decision	Substantially Equivalent
Regulation	892.1710

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View the full FDA submission: accessdata.fda.gov

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PLANMED SOPHIE NUANCE CLASSIC

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