FDA 510(k) Applications for Medical Device Product Code "MQA"
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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 |