Xario 200 Diagnostic Ultrasound System V6.0
K-Number: K172276 · 2017-12-12
Device Summary
Frequently Asked Questions
What is the Xario 200 Diagnostic Ultrasound System V6.0?
Xario 200 Diagnostic Ultrasound System V6.0 is a medical device that received FDA 510(k) clearance on 2017-12-12. The listed applicant is Toshibamedical Systems Corporation. The 510(k) number is K172276.
When did Xario 200 Diagnostic Ultrasound System V6.0 receive FDA 510(k) clearance?
Xario 200 Diagnostic Ultrasound System V6.0 received FDA 510(k) clearance on 2017-12-12, under 510(k) number K172276.
Who is the listed applicant for Xario 200 Diagnostic Ultrasound System V6.0?
The FDA 510(k) record lists Toshibamedical Systems Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Xario 200 Diagnostic Ultrasound System V6.0?
The FDA product code for Xario 200 Diagnostic Ultrasound System V6.0 is IYN.
Other records listing Toshibamedical Systems Corporation 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.