K-number	K091039
Device name	KOWA, FM-600, MODEL LSS50
Applicant	Kowa Co. , Ltd.
Product code	MYC
Device class	Class II
Decision date	Aug 7, 2009
Decision	Substantially Equivalent
Regulation	886.1570

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View the full FDA submission: accessdata.fda.gov

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KOWA, FM-600, MODEL LSS50

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