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FDA 510(k)

CARTO 3 EP Navigation System, Version 7.1 and Accessories

K-Number: K191660 · 2019-07-20

Decision Date2019-07-20
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARTO 3 EP Navigation System, Version 7.1 and Accessories is a medical device manufactured by Biosense Webster, Inc.. It received FDA 510(k) clearance on 2019-07-20 under approval number K191660. 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 7.1 and Accessories?

CARTO 3 EP Navigation System, Version 7.1 and Accessories is a medical device that received FDA 510(k) clearance on 2019-07-20. It is manufactured by Biosense Webster, Inc.. The 510(k) number is K191660.

When was CARTO 3 EP Navigation System, Version 7.1 and Accessories approved by the FDA?

CARTO 3 EP Navigation System, Version 7.1 and Accessories received FDA 510(k) clearance on 2019-07-20, under approval number K191660.

What company makes CARTO 3 EP Navigation System, Version 7.1 and Accessories?

CARTO 3 EP Navigation System, Version 7.1 and Accessories is manufactured by Biosense Webster, Inc..

What is the FDA product code for CARTO 3 EP Navigation System, Version 7.1 and Accessories?

The FDA product code for CARTO 3 EP Navigation System, Version 7.1 and Accessories is DQK.

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Official Source

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