FDA 510(k) Applications for Medical Device Product Code "DBJ"
(Antiparietal Antibody, Indirect Immunofluorescent, Antigen, Control)

FDA 510(k) Number Applicant Device Name Decision Date
K930422 ELIAS USA, INC. SYNELISA PARIETAL CELL ANTIBODIES 08/03/1993
K790759 MEDICA CORP. IIF-APCA TEST KIT 07/30/1979


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