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FDA 510(k) Applications Submitted by OREX COMPUTED RADIOGRAPHY LTD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K073670
12/27/2007
KODAK POINT OF CARE CR 120, KODAK POINT OF CARE CR 140, KODAK POINT OF CARE CR 260
OREX COMPUTED RADIOGRAPHY LTD
K032654
08/28/2003
PORT CASSETTE
OREX COMPUTED RADIOGRAPHY LTD
K003256
10/17/2000
PCCR DIGITAL IMAGING DEVICE
OREX COMPUTED RADIOGRAPHY LTD
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