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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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