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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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