Intl. Diagnostic Technology
FDA 510(k) & PMA Approved Devices — 29 products
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Total Devices29
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K850591 | FIAX TOXO-M ANTIBODIES TEST KIT | GLZ | 1985-04-30 | View |
| 510(k) | K843570 | FIAX HAPTOGLOBIN TEST KIT | DAB | 1984-10-05 | View |
| 510(k) | K843621 | FIAX 420 DILUTOR | JQW | 1984-09-28 | View |
| 510(k) | K843356 | FIAX 100 FLUOROMETER | JZT | 1984-09-17 | View |
| 510(k) | K842749 | FIAX TOTAL IGE TEST KIT | DGP | 1984-08-28 | View |
| 510(k) | K842071 | FIAX TRANSFERRIN TEST KIT | DDI | 1984-07-11 | View |
| 510(k) | K841174 | RUBELLA ANTIBODY FLUOROIMMUNOASSAY | GOL | 1984-06-07 | View |
| 510(k) | K840867 | ALPHA-1-ANTITRYPSIN, FITC, ANTIGEN | DEI | 1984-05-11 | View |
| 510(k) | K834140 | ANTINUCLEAR ANTIBODY IMMUNOLOGICAL SYS | KTL | 1984-01-20 | View |
| 510(k) | K833984 | ANTINUCLEAR ANTIBODY IMMUNOLOGICAL | KTL | 1984-01-04 | View |
| 510(k) | K832821 | FIAX IGG TEST | DFI | 1983-10-14 | View |
| 510(k) | K832383 | IDT ANA STIQ ASSAY | DHN | 1983-08-31 | View |
| 510(k) | K832054 | FIAX CRP TEST KIT | DCK | 1983-08-26 | View |
| 510(k) | K831607 | FIAX IGA TEST KIT | CZN | 1983-06-22 | View |
| 510(k) | K831608 | FIAX IGM TEST KIT | DFT | 1983-06-22 | View |
| 510(k) | K831609 | FIAX IGG TEST KIT | DGK | 1983-06-17 | View |
| 510(k) | K830669 | FIAX COMPLEMENT C4 TEST KIT | DBI | 1983-04-08 | View |
| 510(k) | K830668 | FIAX COMPLEMENT C3 TEST KIT | CZW | 1983-04-05 | View |
| 510(k) | K812968 | FIAX RHEUMATOID FACTOR TEST KIT | DHR | 1981-11-06 | View |
| 510(k) | K801642 | FIAX TEST KIT FOR THEOPHYLLINE QUANT. | KLS | 1980-08-27 | View |
No matching devices.
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