K-number	K923915
Device name	TORQR SERIES DIAGNOSTIC EP CATHETERS
Applicant	Cardiorhythm
Product code	DRF
Device class	Class II
Decision date	Feb 10, 1993
Decision	Substantially Equivalent
Regulation	870.1220

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Source

View the full FDA submission: accessdata.fda.gov

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TORQR SERIES DIAGNOSTIC EP CATHETERS

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