Vivid E80, Vivid E90, Vivid E95
K-Number: K220882 · 2022-07-22
ApplicantGe Medical Systems Ultrasound And
Decision Date2022-07-22
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Vivid E80, Vivid E90, Vivid E95 is a medical device manufactured by Ge Medical Systems Ultrasound And. It received FDA 510(k) clearance on 2022-07-22 under approval number K220882. 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 E80, Vivid E90, Vivid E95?
Vivid E80, Vivid E90, Vivid E95 is a medical device that received FDA 510(k) clearance on 2022-07-22. It is manufactured by Ge Medical Systems Ultrasound And. The 510(k) number is K220882.
When was Vivid E80, Vivid E90, Vivid E95 approved by the FDA?
Vivid E80, Vivid E90, Vivid E95 received FDA 510(k) clearance on 2022-07-22, under approval number K220882.
What company makes Vivid E80, Vivid E90, Vivid E95?
Vivid E80, Vivid E90, Vivid E95 is manufactured by Ge Medical Systems Ultrasound And.
What is the FDA product code for Vivid E80, Vivid E90, Vivid E95?
The FDA product code for Vivid E80, Vivid E90, Vivid E95 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.