K-number	K143481
Device name	IntellaMap Orion High Resolution Mapping Catheter
Applicant	Rhythmia Medical, Inc.
Product code	DRF
Device class	Class II
Decision date	Jan 8, 2015
Decision	Substantially Equivalent
Regulation	870.1220

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Source

View the full FDA submission: accessdata.fda.gov

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IntellaMap Orion High Resolution Mapping Catheter

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