HD80 Series Ultrasound Diagnostic System
K-Number: K233841 · 2024-05-16
Device Summary
Frequently Asked Questions
What is the HD80 Series Ultrasound Diagnostic System?
HD80 Series Ultrasound Diagnostic System is a medical device that received FDA 510(k) clearance on 2024-05-16. The listed applicant is Qingdao Hisense Medical Equipment Co., Ltd.. The 510(k) number is K233841.
When did HD80 Series Ultrasound Diagnostic System receive FDA 510(k) clearance?
HD80 Series Ultrasound Diagnostic System received FDA 510(k) clearance on 2024-05-16, under 510(k) number K233841.
Who is the listed applicant for HD80 Series Ultrasound Diagnostic System?
The FDA 510(k) record lists Qingdao Hisense Medical Equipment Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HD80 Series Ultrasound Diagnostic System?
The FDA product code for HD80 Series Ultrasound Diagnostic 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 Qingdao Hisense Medical Equipment 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.