K-number	K001347
Device name	MERIDIAN-II AND MERDIAN-PLUS
Applicant	Meridian Co., Ltd.
Product code	GZO
Device class	Class II
Decision date	Nov 3, 2000
Decision	Substantially Equivalent
Regulation	882.1540

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View the full FDA submission: accessdata.fda.gov

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MERIDIAN-II AND MERDIAN-PLUS

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