K-number	K924095
Device name	TIMEOSCOPE AND FLEXISCOPE
Applicant	Stethoscopes of America, Inc.
Product code	LDE
Device class	Class I
Decision date	Oct 20, 1992
Decision	Substantially Equivalent
Regulation	870.1875

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View the full FDA submission: accessdata.fda.gov

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TIMEOSCOPE AND FLEXISCOPE

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