DIGITAL RADIOGRAPHY SYSTEM WITH FLAT PANEL DETECTOR, MODEL DFP8000D— 510(k) K041027

Name: FDA 510(k) clearance K041027
Creator: U.S. Food and Drug Administration
Published: 2004-05-14

Substantially Equivalent

Toshibamedical Systems Corporation

FDA 510(k) clearance K041027 for DIGITAL RADIOGRAPHY SYSTEM WITH FLAT PANEL DETECTOR, MODEL DFP8000D, Substantially Equivalent on 2004-05-14. Applicant: Toshibamedical Systems Corporation. Device class: 2.

Clearance details

Applicant: Toshibamedical Systems Corporation
Product code: Code IZI
Device class: Class 2
Regulation: 21 CFR 892.1600
Advisory panel: Radiology
Date received: 2004-04-21
Decision date: 2004-05-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tustin, CA, US

Download summary PDF View on FDA.gov ↗

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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.