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FDA 510(k)

CARTO 3 EP Navigation System, Version 5.2 and Accessories with CARTOFINDER Module

K-Number: K173978 · 2018-08-24

Decision Date2018-08-24
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARTO 3 EP Navigation System, Version 5.2 and Accessories with CARTOFINDER Module is a medical device manufactured by Biosense Webster, Inc.. It received FDA 510(k) clearance on 2018-08-24 under approval number K173978. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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.

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Official Source

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