DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM— 510(k) K110999

Substantially Equivalent

Edan Instruments, Inc.

FDA 510(k) clearance K110999 for DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM, Substantially Equivalent on 2011-04-26. Applicant: Edan Instruments, Inc..

Clearance details

Applicant: Edan Instruments, Inc.
Product code: Code ITX
Advisory panel: Radiology
Date received: 2011-04-11
Decision date: 2011-04-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nanshan, Guangdong, CN

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Adverse events under product code ITX

product code ITX

Death: 6
Injury: 137
Malfunction: 2,036
Total: 2,179

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.