K-number	K172503
Device name	MR Conditional Cup Electrode, MR Conditional Webb Electrode
Applicant	Rhythmlink International, LLC
Product code	GXY
Device class	Class II
Decision date	Dec 1, 2017
Decision	Substantially Equivalent
Regulation	882.1320

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Source

View the full FDA submission: accessdata.fda.gov

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MR Conditional Cup Electrode, MR Conditional Webb Electrode

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