CARTO 3 EP Navigation System, Version 5.2 and Accessories with CARTOFINDER Module
K-Number: K173978 · 2018-08-24
Device Summary
Frequently Asked Questions
What is the CARTO 3 EP Navigation System, Version 5.2 and Accessories with CARTOFINDER Module?
CARTO 3 EP Navigation System, Version 5.2 and Accessories with CARTOFINDER Module is a medical device that received FDA 510(k) clearance on 2018-08-24. It is manufactured by Biosense Webster, Inc.. The 510(k) number is K173978.
When was CARTO 3 EP Navigation System, Version 5.2 and Accessories with CARTOFINDER Module approved by the FDA?
CARTO 3 EP Navigation System, Version 5.2 and Accessories with CARTOFINDER Module received FDA 510(k) clearance on 2018-08-24, under approval number K173978.
What company makes CARTO 3 EP Navigation System, Version 5.2 and Accessories with CARTOFINDER Module?
CARTO 3 EP Navigation System, Version 5.2 and Accessories with CARTOFINDER Module is manufactured by Biosense Webster, Inc..
What is the FDA product code for CARTO 3 EP Navigation System, Version 5.2 and Accessories with CARTOFINDER Module?
The FDA product code for CARTO 3 EP Navigation System, Version 5.2 and Accessories with CARTOFINDER Module is DQK.
Related Clinical Trials
Related PubMed Literature
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Official Source
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