K-number	K160390
Device name	Map-it Diagnostic Mapping Catheters
Applicant	Access Point Technologies Ep, Inc.
Product code	DRF
Device class	Class II
Decision date	Apr 11, 2016
Decision	Substantially Equivalent
Regulation	870.1220

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Source

View the full FDA submission: accessdata.fda.gov

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Map-it Diagnostic Mapping Catheters

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