K-number	K000510
Device name	ART-M1, MODEL M1-1-ART-A1
Applicant	Bonart Co., Ltd.
Product code	ELC
Device class	Class II
Decision date	May 15, 2000
Decision	Substantially Equivalent
Regulation	872.4850

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View the full FDA submission: accessdata.fda.gov

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ART-M1, MODEL M1-1-ART-A1

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