FDA 510(k) Applications for Medical Device Product Code "MQA"
(Anti-Ribosomal P Antibodies)

FDA 510(k) Number Applicant Device Name Decision Date
K950169 HOGAN & HARTSON RIBOSOMAL P EIA TEST SYSTEM 05/23/1996
K981237 INOVA DIAGNOSTICS, INC. QUANTA LITE RIBOSOME P ELISA 06/05/1998
K202540 Phadia AB EliA Rib-P 09/13/2021
K024151 THERATEST LABORATORIES, INC. EL-ANA PROFILES: ANTI-RIBOSOMAL PROTEIN P 02/06/2003


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