SONOTOUCH SERIES DIAGNOSTIC ULTRASOUND SYSTEMS
K-Number: K121867 · 2012-08-02
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Device Summary
Frequently Asked Questions
What is the SONOTOUCH SERIES DIAGNOSTIC ULTRASOUND SYSTEMS?
SONOTOUCH SERIES DIAGNOSTIC ULTRASOUND SYSTEMS is a medical device that received FDA 510(k) clearance on 2012-08-02. The listed applicant is Chison Medical Imaging Co., Ltd.. The 510(k) number is K121867.
When did SONOTOUCH SERIES DIAGNOSTIC ULTRASOUND SYSTEMS receive FDA 510(k) clearance?
SONOTOUCH SERIES DIAGNOSTIC ULTRASOUND SYSTEMS received FDA 510(k) clearance on 2012-08-02, under 510(k) number K121867.
Who is the listed applicant for SONOTOUCH SERIES DIAGNOSTIC ULTRASOUND SYSTEMS?
The FDA 510(k) record lists Chison Medical Imaging Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SONOTOUCH SERIES DIAGNOSTIC ULTRASOUND SYSTEMS?
The FDA product code for SONOTOUCH SERIES DIAGNOSTIC ULTRASOUND SYSTEMS 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 Chison Medical Imaging 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.
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