KODAK EKTACHEM DTII SYSTEM— 510(k) K912844

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K912844 for KODAK EKTACHEM DTII SYSTEM, Substantially Equivalent on 1991-09-04. Applicant: Eastman Kodak Company.

Clearance details

Applicant: Eastman Kodak Company
Product code: Code JJE
Advisory panel: Clinical Chemistry
Date received: 1991-06-26
Decision date: 1991-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

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Adverse events under product code JJE

product code JJE

Death: 6
Injury: 441
Malfunction: 25,011
Other: 1
Total: 25,459

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.