GE TETHERED PORTABLE DIGITAL RADIOGRAPHIC DETECTOR— 510(k) K041922

Name: FDA 510(k) clearance K041922
Creator: U.S. Food and Drug Administration
Published: 2004-07-28

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K041922 for GE TETHERED PORTABLE DIGITAL RADIOGRAPHIC DETECTOR, Substantially Equivalent on 2004-07-28. Applicant: General Electric Co.. Device class: 2.

Clearance details

Applicant: General Electric Co.
Product code: Code IZL
Device class: Class 2
Regulation: 21 CFR 892.1720
Advisory panel: Radiology
Date received: 2004-07-16
Decision date: 2004-07-28
Decision: Substantially Equivalent
Clearance type: Special
Location: Milwaukee, WI, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code IZL

product code IZL

Other: 3
Total: 3

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.