K-number	K770988
Device name	FOAM ECG ELECTRODE, 2060 AND 2061
Applicant	Cardio-Dynamics Laboratories, Inc.
Product code	DRX
Device class	Class II
Decision date	Jun 14, 1977
Decision	Substantially Equivalent
Regulation	870.2360

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View the full FDA submission: accessdata.fda.gov

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FOAM ECG ELECTRODE, 2060 AND 2061

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