K-number	K990809
Device name	CADISCOPE ELECTRONIC STETHOSCOPE
Applicant	Caditec AG
Product code	DQD
Device class	Class II
Decision date	Jun 9, 1999
Decision	Substantially Equivalent
Regulation	870.1875

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View the full FDA submission: accessdata.fda.gov

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CADISCOPE ELECTRONIC STETHOSCOPE

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