K-number	K964272
Device name	PERFORMR SERIES EP DIAGNOSTIC CATHETERS
Applicant	Medtronic Cardiorhythm
Product code	DRF
Device class	Class II
Decision date	Jan 23, 1997
Decision	Substantially Equivalent
Regulation	870.1220

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Source

View the full FDA submission: accessdata.fda.gov

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PERFORMR SERIES EP DIAGNOSTIC CATHETERS

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