Vivid E80/ Vivid E90/ Vivid E95
K-Number: K200743 · 2020-07-23
ApplicantGe Medical Systems Ultrasound And
Decision Date2020-07-23
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 2020-07-23 under approval number K200743. 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 2020-07-23. It is manufactured by Ge Medical Systems Ultrasound And. The 510(k) number is K200743.
When was Vivid E80/ Vivid E90/ Vivid E95 approved by the FDA?
Vivid E80/ Vivid E90/ Vivid E95 received FDA 510(k) clearance on 2020-07-23, under approval number K200743.
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.