GE ECHOPAC— 510(k) K123894

Substantially Equivalent

Ge Vingmed Ultrasound AS

FDA 510(k) clearance K123894 for GE ECHOPAC, Substantially Equivalent on 2013-01-29. Applicant: Ge Vingmed Ultrasound AS.

Clearance details

Applicant: Ge Vingmed Ultrasound AS
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2012-12-18
Decision date: 2013-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wauwatosa, WI, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

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.