FDA 510(k) Applications for Medical Device Product Code "DFI"
(Total Spinal-Fluid, Antigen, Antiserum, Control)

FDA 510(k) Number Applicant Device Name Decision Date
K854190 CANYON DIAGNOSTICS, INC. CANTROL SPINAL FLUID CONTROL 11/25/1985
K832821 INTL. DIAGNOSTIC TECHNOLOGY FIAX IGG TEST 10/14/1983
K843122 ISOLAB, INC. RESOLVE-CSF 11/30/1984
K840974 SOMAS MEDICAL INDUSTRIES, INC. SOMAS HUMAN SPINAL FLUID CONTROL 04/05/1984


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