FDA 510(k) Applications Submitted by AGEN BIOMEDICAL LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K993276 09/30/1999 SIMPLIFY D-DIMER, MODEL DCGK1 AGEN BIOMEDICAL LTD.
K974596 12/09/1997 DIMERTEST LATEX ASSAY AGEN BIOMEDICAL LTD.


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