K-number	K221879
Device name	Patient Monitor, models LM-8, LM-10, LM-12 and LM-15
Applicant	Caf Medical Solutions, Inc.
Product code	MHX
Device class	Class II
Decision date	Aug 10, 2022
Decision	Substantially Equivalent
Regulation	870.1025

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Source

View the full FDA submission: accessdata.fda.gov

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Patient Monitor, models LM-8, LM-10, LM-12 and LM-15

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