K-number	K954389
Device name	CONMED ECG/EKG ELECTRODES
Applicant	Conmedcorp
Product code	DRX
Device class	Class II
Decision date	May 16, 1996
Decision	Substantially Equivalent
Regulation	870.2360

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View the full FDA submission: accessdata.fda.gov

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CONMED ECG/EKG ELECTRODES

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