K-number	K100217
Device name	LUCON M-SERIES PATIENT MONITOR, MODELS M20 AND M30
Applicant	Mediana Co., Ltd.
Product code	MHX
Device class	Class II
Decision date	Jun 8, 2010
Decision	Substantially Equivalent
Regulation	870.1025

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View the full FDA submission: accessdata.fda.gov

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LUCON M-SERIES PATIENT MONITOR, MODELS M20 AND M30

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