CARTO 3 EP Navigation System, Version 6.0 and Accessories
K-Number: K170600 · 2017-07-25
Device Summary
Frequently Asked Questions
What is the CARTO 3 EP Navigation System, Version 6.0 and Accessories?
CARTO 3 EP Navigation System, Version 6.0 and Accessories is a medical device that received FDA 510(k) clearance on 2017-07-25. It is manufactured by Biosense Webster, Inc.. The 510(k) number is K170600.
When was CARTO 3 EP Navigation System, Version 6.0 and Accessories approved by the FDA?
CARTO 3 EP Navigation System, Version 6.0 and Accessories received FDA 510(k) clearance on 2017-07-25, under approval number K170600.
What company makes CARTO 3 EP Navigation System, Version 6.0 and Accessories?
CARTO 3 EP Navigation System, Version 6.0 and Accessories is manufactured by Biosense Webster, Inc..
What is the FDA product code for CARTO 3 EP Navigation System, Version 6.0 and Accessories?
The FDA product code for CARTO 3 EP Navigation System, Version 6.0 and Accessories is DQK.
Related Clinical Trials
Related PubMed Literature
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.