Eastman Kodak Company - FDA 510(k) Cleared Devices
Recent clearances: KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80KW GENERATORS, MODELS 6551345, 6551386, KODAK ECLIPSE IMAGE PROCESSING SOFTWARE, KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEM
238
Total
238
Cleared
0
Denied
FDA 510(k) Regulatory Record - Eastman Kodak Company Cardiovascular ✕
2 devices