K-number	K160242
Device name	Reprocessed Livewire Steerable Diagnostic EP Catheter
Applicant	Innovative Health, LLC
Product code	NLH
Device class	Class II
Decision date	May 10, 2016
Decision	Substantially Equivalent
Regulation	870.1220

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Source

View the full FDA submission: accessdata.fda.gov

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Reprocessed Livewire Steerable Diagnostic EP Catheter

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