K-number	K831878
Device name	CARDIO-SCOPE MINI MONITOR
Applicant	W.E. Leder Enterprises, Inc.
Product code	DPS
Device class	Class II
Decision date	Sep 29, 1983
Decision	Substantially Equivalent
Regulation	870.2340

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View the full FDA submission: accessdata.fda.gov

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CARDIO-SCOPE MINI MONITOR

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