Vivid S60N, Vivid S70N
K-Number: K200497 · 2020-07-16
Device Summary
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 2020-07-16. The listed applicant is GE Medical Systems Ultrasound and Primary Care Diagnostics. The 510(k) number is K200497.
When did Vivid S60N, Vivid S70N receive FDA 510(k) clearance?
Vivid S60N, Vivid S70N received FDA 510(k) clearance on 2020-07-16, under 510(k) number K200497.
Who is the listed applicant for Vivid S60N, Vivid S70N?
The FDA 510(k) record lists GE Medical Systems Ultrasound and Primary Care Diagnostics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vivid S60N, Vivid S70N?
The FDA product code for Vivid S60N, Vivid S70N is IYN.
Other records listing GE Medical Systems Ultrasound and Primary Care Diagnostics as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: IYN)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.