ZS3 Ultrasound System, z.one pro Ultrasound System
K-Number: K171891 · 2017-09-21
Device Summary
Frequently Asked Questions
What is the ZS3 Ultrasound System, z.one pro Ultrasound System?
ZS3 Ultrasound System, z.one pro Ultrasound System is a medical device that received FDA 510(k) clearance on 2017-09-21. The listed applicant is Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. The 510(k) number is K171891.
When did ZS3 Ultrasound System, z.one pro Ultrasound System receive FDA 510(k) clearance?
ZS3 Ultrasound System, z.one pro Ultrasound System received FDA 510(k) clearance on 2017-09-21, under 510(k) number K171891.
Who is the listed applicant for ZS3 Ultrasound System, z.one pro Ultrasound System?
The FDA 510(k) record lists Shenzhen Mindray Bio-Medical Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ZS3 Ultrasound System, z.one pro Ultrasound System?
The FDA product code for ZS3 Ultrasound System, z.one pro Ultrasound System is IYN.
Other records listing Shenzhen Mindray Bio-Medical Electronics 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.