Vivid S60N, Vivid S70N
K-Number: K223832 · 2023-02-16
Decision Date2023-02-16
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Vivid S60N, Vivid S70N is a medical device manufactured by Ge Medical System Ultrasound and Primary Care Diagnostics. It received FDA 510(k) clearance on 2023-02-16 under approval number K223832. 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 S60N, Vivid S70N?
Vivid S60N, Vivid S70N is a medical device that received FDA 510(k) clearance on 2023-02-16. It is manufactured by Ge Medical System Ultrasound and Primary Care Diagnostics. The 510(k) number is K223832.
When was Vivid S60N, Vivid S70N approved by the FDA?
Vivid S60N, Vivid S70N received FDA 510(k) clearance on 2023-02-16, under approval number K223832.
What company makes Vivid S60N, Vivid S70N?
Vivid S60N, Vivid S70N is manufactured by Ge Medical System Ultrasound and Primary Care Diagnostics.
What is the FDA product code for Vivid S60N, Vivid S70N?
The FDA product code for Vivid S60N, Vivid S70N is IYN.
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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.