Carnation series Diagnostic Ultrasound System
K-Number: K230066 · 2023-09-15
Device Summary
Frequently Asked Questions
What is the Carnation series Diagnostic Ultrasound System?
Carnation series Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2023-09-15. The listed applicant is Shenzhen Wisonic Medical Technology Co. , Ltd.. The 510(k) number is K230066.
When did Carnation series Diagnostic Ultrasound System receive FDA 510(k) clearance?
Carnation series Diagnostic Ultrasound System received FDA 510(k) clearance on 2023-09-15, under 510(k) number K230066.
Who is the listed applicant for Carnation series Diagnostic Ultrasound System?
The FDA 510(k) record lists Shenzhen Wisonic Medical Technology Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Carnation series Diagnostic Ultrasound System?
The FDA product code for Carnation series Diagnostic Ultrasound System is IYN.
Related Clinical Trials
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.
Other records listing Shenzhen Wisonic Medical Technology Co. , Ltd. 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.