K-number	K130220
Device name	MR CONDITIONAL PRESSON ELECTRODE
Applicant	Rhythmlink International, LLC
Product code	GXZ
Device class	Class II
Decision date	Jul 22, 2013
Decision	Substantially Equivalent
Regulation	882.1350

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Source

View the full FDA submission: accessdata.fda.gov

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MR CONDITIONAL PRESSON ELECTRODE

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