FDA 510(k) Applications Submitted by ANALYTICON BIOTECHNOLOGIES AG

FDA 510(k) Number Submission Date Device Name Applicant
K023885 11/21/2002 COMBI-SCREEN, MODELS 10SL AND 11SL ANALYTICON BIOTECHNOLOGIES AG
K061812 06/26/2006 COMBI SCAN 500 URINE TEST STRIP ANALYZER, MODEL A93005 ANALYTICON BIOTECHNOLOGIES AG
K061846 06/26/2006 COMBI SCAN100 ANALYTICON BIOTECHNOLOGIES AG


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