K-number	K120193
Device name	ANY VIEW PATIENT MONITORS
Applicant	Guangdong Biolight Meditech Co., Ltd.
Product code	MWI
Device class	Class II
Decision date	Jun 29, 2012
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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ANY VIEW PATIENT MONITORS

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