COMPAS— 510(k) K945483

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K945483 for COMPAS, Substantially Equivalent on 1994-12-09. Applicant: General Electric Co..

Clearance details

Applicant: General Electric Co.
Product code: Code IZI
Advisory panel: Radiology
Date received: 1994-11-08
Decision date: 1994-12-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milwaukee, WI, US

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Adverse events under product code IZI

product code IZI

Death: 9
Malfunction: 5,312
Total: 5,321

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.