Hi-Light Diagnostic Ultrasound Systems— 510(k) K151709

Substantially Equivalent

Qingdao Hisense Medical Equipment Co., Ltd.

FDA 510(k) clearance K151709 for Hi-Light Diagnostic Ultrasound Systems, Substantially Equivalent on 2015-07-17. Applicant: Qingdao Hisense Medical Equipment Co., Ltd..

Clearance details

Applicant: Qingdao Hisense Medical Equipment Co., Ltd.
Product code: Code IYO
Advisory panel: Radiology
Date received: 2015-06-24
Decision date: 2015-07-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Qingdao, CN

Download summary PDF View on FDA.gov ↗

Adverse events under product code IYO

product code IYO

Malfunction: 3,339
Total: 3,339

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.