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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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