DICOM IMAGE MANAGER, MODEL 3-D VISUALIZATION OPTION— 510(k) K990248

Substantially Equivalent

Dicomit Imaging Systems Corp.

FDA 510(k) clearance K990248 for DICOM IMAGE MANAGER, MODEL 3-D VISUALIZATION OPTION, Substantially Equivalent on 1999-04-16. Applicant: Dicomit Imaging Systems Corp..

Clearance details

Applicant: Dicomit Imaging Systems Corp.
Product code: Code IYO
Advisory panel: Radiology
Date received: 1999-01-26
Decision date: 1999-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Richmond Hill, Ontario, CA

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Adverse events under product code IYO

product code IYO

Malfunction: 3,339
Total: 3,339

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.