K-number	K201941
Device name	Monitor B125, Monitor B105
Applicant	Ge Medical Systems Information Technologies, Inc.
Product code	MHX
Device class	Class II
Decision date	Nov 4, 2020
Decision	Substantially Equivalent
Regulation	870.1025

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Source

View the full FDA submission: accessdata.fda.gov

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Monitor B125, Monitor B105

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