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FDA 510(k)

Foresight Intracardiac Echocardiology (ICE) System

K-Number: K162789 · 2017-03-28

ApplicantConavi Medical, Inc.
Decision Date2017-03-28
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Foresight Intracardiac Echocardiology (ICE) System is a medical device manufactured by Conavi Medical, Inc.. It received FDA 510(k) clearance on 2017-03-28 under approval number K162789. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Foresight Intracardiac Echocardiology (ICE) System?

Foresight Intracardiac Echocardiology (ICE) System is a medical device that received FDA 510(k) clearance on 2017-03-28. It is manufactured by Conavi Medical, Inc.. The 510(k) number is K162789.

When was Foresight Intracardiac Echocardiology (ICE) System approved by the FDA?

Foresight Intracardiac Echocardiology (ICE) System received FDA 510(k) clearance on 2017-03-28, under approval number K162789.

What company makes Foresight Intracardiac Echocardiology (ICE) System?

Foresight Intracardiac Echocardiology (ICE) System is manufactured by Conavi Medical, Inc..

What is the FDA product code for Foresight Intracardiac Echocardiology (ICE) System?

The FDA product code for Foresight Intracardiac Echocardiology (ICE) System is DQO.

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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.

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