FDA 510(k) Applications for Medical Device Product Code "LJB"
(Enzyme Linked Immunoabsorbent Assay, Rubeola)

FDA 510(k) Number Applicant Device Name Decision Date
K974552 DIAMEDIX CORP. DIAMEDIX IS-MEASLES IGG TEST SYSTEM 01/28/1998
K971620 INOVA DIAGNOSTICS, INC. QUANTA LITE RUBEOLA (MEASLES) IGG 07/22/1997


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