EBit Series Diagnostic Ultrasound System
K-Number: K162172 · 2016-09-14
Device Summary
Frequently Asked Questions
What is the EBit Series Diagnostic Ultrasound System?
EBit Series Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2016-09-14. The listed applicant is Chison Medical Imaging Co., Ltd.. The 510(k) number is K162172.
When did EBit Series Diagnostic Ultrasound System receive FDA 510(k) clearance?
EBit Series Diagnostic Ultrasound System received FDA 510(k) clearance on 2016-09-14, under 510(k) number K162172.
Who is the listed applicant for EBit Series Diagnostic Ultrasound System?
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 EBit Series Diagnostic Ultrasound System?
The FDA product code for EBit 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 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.