K-number	K062481
Device name	SERENO ELECTRONIC STETHOSCOPE
Applicant	Pishon High Tech Co., Ltd.
Product code	DQD
Device class	Class II
Decision date	Oct 16, 2006
Decision	Substantially Equivalent
Regulation	870.1875

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View the full FDA submission: accessdata.fda.gov

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SERENO ELECTRONIC STETHOSCOPE

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