CARTO 3 EP Navigation System Version 7.2
K-Number: K213264 · 2021-10-29
Device Summary
Frequently Asked Questions
What is the CARTO 3 EP Navigation System Version 7.2?
CARTO 3 EP Navigation System Version 7.2 is a medical device that received FDA 510(k) clearance on 2021-10-29. It is manufactured by Biosense Webster, Inc.. The 510(k) number is K213264.
When was CARTO 3 EP Navigation System Version 7.2 approved by the FDA?
CARTO 3 EP Navigation System Version 7.2 received FDA 510(k) clearance on 2021-10-29, under approval number K213264.
What company makes CARTO 3 EP Navigation System Version 7.2?
CARTO 3 EP Navigation System Version 7.2 is manufactured by Biosense Webster, Inc..
What is the FDA product code for CARTO 3 EP Navigation System Version 7.2?
The FDA product code for CARTO 3 EP Navigation System Version 7.2 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.