Vivid iq
K-Number: K200708 · 2020-09-09
ApplicantGe Medical Systems Ultrasound And
Decision Date2020-09-09
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Vivid iq is a medical device manufactured by Ge Medical Systems Ultrasound And. It received FDA 510(k) clearance on 2020-09-09 under approval number K200708. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Vivid iq?
Vivid iq is a medical device that received FDA 510(k) clearance on 2020-09-09. It is manufactured by Ge Medical Systems Ultrasound And. The 510(k) number is K200708.
When was Vivid iq approved by the FDA?
Vivid iq received FDA 510(k) clearance on 2020-09-09, under approval number K200708.
What company makes Vivid iq?
Vivid iq is manufactured by Ge Medical Systems Ultrasound And.
What is the FDA product code for Vivid iq?
The FDA product code for Vivid iq is IYN.
Other Devices by Ge Medical Systems Ultrasound And
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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.