K-number	K203261
Device name	Reprocessed Inquiry Steerable Diagnostic EP Catheter
Applicant	Innovative Health, LLC
Product code	DRF
Device class	Class II
Decision date	Mar 5, 2021
Decision	Substantially Equivalent
Regulation	870.1220

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Source

View the full FDA submission: accessdata.fda.gov

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Reprocessed Inquiry Steerable Diagnostic EP Catheter

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