KODAK DIGITAL SCIENCE CARDIAC VIEWER— 510(k) K974086

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K974086 for KODAK DIGITAL SCIENCE CARDIAC VIEWER, Substantially Equivalent on 1998-01-20. Applicant: Eastman Kodak Company.

Clearance details

Applicant: Eastman Kodak Company
Product code: Code LLZ
Advisory panel: Radiology
Date received: 1997-10-29
Decision date: 1998-01-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

Download summary PDF View on FDA.gov ↗

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.