AMX4-50 AND AMX4-31 MOBILE DIGITAL DIAGNOSTIC RADIOGRAPHIC SYSTEMS— 510(k) K063262

Substantially Equivalent

Virtual Imaging

FDA 510(k) clearance K063262 for AMX4-50 AND AMX4-31 MOBILE DIGITAL DIAGNOSTIC RADIOGRAPHIC SYSTEMS, Substantially Equivalent on 2006-12-26. Applicant: Virtual Imaging.

Clearance details

Applicant: Virtual Imaging
Product code: Code IZL
Advisory panel: Radiology
Date received: 2006-10-30
Decision date: 2006-12-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deer Field, IL, US

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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.