KODAK DIGITAL SCIENCE MEDICAL PRINTER INTERFACE UNIT— 510(k) K961740

Substantially Equivalent

Kodak Health Imaging Systems, Inc.

FDA 510(k) clearance K961740 for KODAK DIGITAL SCIENCE MEDICAL PRINTER INTERFACE UNIT, Substantially Equivalent on 1996-11-14. Applicant: Kodak Health Imaging Systems, Inc..

Clearance details

Applicant: Kodak Health Imaging Systems, Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 1996-05-03
Decision date: 1996-11-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, US

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Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

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.