GE VIVID S5 AND S6 DIAGNOSTIC ULTRASOUND— 510(k) K071985

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K071985 for GE VIVID S5 AND S6 DIAGNOSTIC ULTRASOUND, Substantially Equivalent on 2007-08-17. Applicant: General Electric Co..

Clearance details

Applicant: General Electric Co.
Product code: Code IYN
Advisory panel: Radiology
Date received: 2007-07-19
Decision date: 2007-08-17
Decision: Substantially Equivalent
Clearance type: Special
Location: Wauwatosa, WI, US

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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.