FDA 510(k) Applications for Medical Device Product Code "NTY"
(System, Test, Fibrin/Fibrinogen Degradation Products For Monitoring Of Colorectal Cancer)

FDA 510(k) Number Applicant Device Name Decision Date
K072901 AMDL, INC. AMDL-ELISA DR-70 (FDP) IMMUNOASSAY, MODEL DR2101 07/01/2008


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