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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