K-number	K232111
Device name	NeoBeat, NeoBeat Mini
Applicant	Laerdal Medical AS
Product code	MWI
Device class	Class II
Decision date	Jun 25, 2024
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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NeoBeat, NeoBeat Mini

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