K-number	K082767
Device name	KOWA NONMYD ALPHA-DIII
Applicant	Kowa Co. , Ltd.
Product code	HKI
Device class	Class II
Decision date	Oct 21, 2008
Decision	Substantially Equivalent
Regulation	886.1120

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View the full FDA submission: accessdata.fda.gov

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KOWA NONMYD ALPHA-DIII

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