FDA 510(k) Applications for Medical Device Product Code "CZQ"
(Bence-Jones Protein, Antigen, Antiserum, Control)

FDA 510(k) Number Applicant Device Name Decision Date
K802284 KALLESTAD LABORATORIES, INC. ANTISERA TO HUMAN FREE LAMBDA LIGHT CH. 10/23/1980
K812327 KALLESTAD LABORATORIES, INC. KAPPA & LAMBDA BENCE JONES CONTROLS 09/01/1981


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