FDA 510(k) Applications for Medical Device Product Code "DCE"
(Fab, Antigen, Antiserum, Control)

FDA 510(k) Number Applicant Device Name Decision Date
K781951 KALLESTAD LABORATORIES, INC. ANTISERA, RHODAMINE CONJUGATED FRAGMENT 02/16/1979
K772128 KALLESTAD LABORATORIES, INC. FLUORESCEIN CONJUGATED 11/22/1977


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