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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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