K-number	K233313
Device name	Keikku Electronic stethoscope
Applicant	Lapsi Health Holding B.V.
Product code	DQD
Device class	Class II
Decision date	Apr 10, 2024
Decision	Substantially Equivalent
Regulation	870.1875

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Source

View the full FDA submission: accessdata.fda.gov

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Keikku Electronic stethoscope

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