KODAK EKTASCAN XLP PRELIMINARY DV2000 INTERFACE— 510(k) K912454

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K912454 for KODAK EKTASCAN XLP PRELIMINARY DV2000 INTERFACE, Substantially Equivalent on 1991-09-27. Applicant: Eastman Kodak Company.

Clearance details

Applicant: Eastman Kodak Company
Product code: Code JAK
Advisory panel: Radiology
Date received: 1991-06-03
Decision date: 1991-09-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

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Adverse events under product code JAK

product code JAK

Death: 27
Injury: 571
Malfunction: 779
Total: 1,377

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.