FDA 510(k) Applications Submitted by EXIGENT DIAGNOSTICS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K980041 01/06/1998 CARESIDE ALBUMIN EXIGENT DIAGNOSTICS, INC.
K980042 01/06/1998 CARESIDE TOTAL PROTEIN EXIGENT DIAGNOSTICS, INC.
K980043 01/06/1998 CARESIDE CREATININE EXIGENT DIAGNOSTICS, INC.
K980055 01/06/1998 CARESIDE GLOBULIN EXIGENT DIAGNOSTICS, INC.
K980056 01/06/1998 CARESIDE ANALYZER EXIGENT DIAGNOSTICS, INC.
K980057 01/06/1998 CARESIDE BUN EXIGENT DIAGNOSTICS, INC.
K981183 04/01/1998 CARESIDE GLUCOSE EXIGENT DIAGNOSTICS, INC.
K981899 06/01/1998 CARESIDE HDL-CHOLESTEROL EXIGENT DIAGNOSTICS, INC.
K982118 06/03/1998 CARESIDE ANALYZER EXIGENT DIAGNOSTICS, INC.


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