K-number	K102721
Device name	LIVEWIRE ELECTOPHYSIOLOGY CATHETER
Applicant	St Jude Medical
Product code	DRF
Device class	Class II
Decision date	Oct 18, 2010
Decision	Substantially Equivalent
Regulation	870.1220

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Source

View the full FDA submission: accessdata.fda.gov

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LIVEWIRE ELECTOPHYSIOLOGY CATHETER

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