GE ECHOPAC— 510(k) K072952

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K072952 for GE ECHOPAC, Substantially Equivalent on 2007-11-16. Applicant: General Electric Co..

Clearance details

Applicant: General Electric Co.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2007-10-18
Decision date: 2007-11-16
Decision: Substantially Equivalent
Clearance type: Special
Location: Wauwatosa, WI, US

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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.