FDA 510(k) Applications Submitted by PHARMACIA DIAGNOSTICS AB

FDA 510(k) Number Submission Date Device Name Applicant
K051218 05/12/2005 MODIFICATION TO: UNICAP SPECIFIC IGE PHARMACIA DIAGNOSTICS AB
K052793 10/03/2005 IMMUNOCAP/UNICAP GLIADIN IGA, IMMUNOCAP/UNICAP SPECIFIC IGA, MODELS 14-4425-40, 10-9306-02 PHARMACIA DIAGNOSTICS AB


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