FDA 510(k) Applications for Medical Device Product Code "NAO"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K992502 | AXIS | AXIS %CDT TURBIDIMETRIC IMMUNOASSAY | 12/21/1999 |
K060677 | DADE BEHRING, INC. | N LATEX CDT | 08/25/2006 |
K001943 | SANGUI BIOTECH, INC. | CHRONALCO I.D.CDT (CARBOHYDRATE DEFICIENT TRANSFERRIN) ASSAY | 08/23/2000 |