Eastman Kodak Company - FDA 510(k) Cleared Devices
238
Total
238
Cleared
0
Denied
Eastman Kodak Company has 238 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 238 cleared submissions from 1977 to 2006. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Eastman Kodak Company Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Eastman Kodak Company
238 devices
Cleared
Mar 31, 2006
KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80KW GENERATORS, MODELS 6551345, 6551386
Radiology
29d
Cleared
Mar 16, 2006
KODAK ECLIPSE IMAGE PROCESSING SOFTWARE
Radiology
56d
Cleared
Feb 08, 2006
KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEM
Radiology
29d
Cleared
Feb 07, 2006
KODAK PACS
Radiology
29d
Cleared
Jan 04, 2006
KODAK CARESTREAM PACS
Radiology
33d
Cleared
Jun 21, 2005
KODAK DIRECTVIEW DR SYSTEM DETECTOR
Radiology
15d
Cleared
Jun 01, 2005
KODAK DIRECTVIEW DR 7500 SYSTEM, MODEL 8791345
Radiology
16d
Cleared
Sep 24, 2004
KODAK MEDICAL IMAGER 300
Radiology
45d
Cleared
Sep 24, 2004
KODAK COLOR MEDICAL IMAGER 1000
Radiology
45d
Cleared
May 24, 2004
KODAK DIRECTVIEW CR CASSETTE/GP/15 X 30 CM, CATALOG# 8418253
Radiology
97d
Cleared
Apr 07, 2004
TROPHYPAN C WITH ORTHOIMAGING/OMSIMAGING ACCESSORY
Radiology
36d
Cleared
Feb 20, 2004
KODAK DRYVIEW 8900 LASER IMAGER MAMMOGRAPHY ACCESSORY
Radiology
73d
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