GE LOGIQ 7, MODEL 2354858— 510(k) K032182

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K032182 for GE LOGIQ 7, MODEL 2354858, Substantially Equivalent on 2003-07-25. Applicant: General Electric Co..

Clearance details

Applicant: General Electric Co.
Product code: Code IYN
Advisory panel: Radiology
Date received: 2003-07-17
Decision date: 2003-07-25
Decision: Substantially Equivalent
Clearance type: Special
Location: Milwaukee, WI, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code IYN

product code IYN

Death: 25
Injury: 163
Malfunction: 1,538
Other: 4
Total: 1,730

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.