Intl. Diagnostic Technology
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 29
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K850591 | FIAX TOXO-M ANTIBODIES TEST KIT | April 30, 1985 |
| K843570 | FIAX HAPTOGLOBIN TEST KIT | October 5, 1984 |
| K843621 | FIAX 420 DILUTOR | September 28, 1984 |
| K843356 | FIAX 100 FLUOROMETER | September 17, 1984 |
| K842749 | FIAX TOTAL IGE TEST KIT | August 28, 1984 |
| K842071 | FIAX TRANSFERRIN TEST KIT | July 11, 1984 |
| K841174 | RUBELLA ANTIBODY FLUOROIMMUNOASSAY | June 7, 1984 |
| K840867 | ALPHA-1-ANTITRYPSIN, FITC, ANTIGEN | May 11, 1984 |
| K834140 | ANTINUCLEAR ANTIBODY IMMUNOLOGICAL SYS | January 20, 1984 |
| K833984 | ANTINUCLEAR ANTIBODY IMMUNOLOGICAL | January 4, 1984 |
| K832821 | FIAX IGG TEST | October 14, 1983 |
| K832383 | IDT ANA STIQ ASSAY | August 31, 1983 |
| K832054 | FIAX CRP TEST KIT | August 26, 1983 |
| K831608 | FIAX IGM TEST KIT | June 22, 1983 |
| K831607 | FIAX IGA TEST KIT | June 22, 1983 |
| K831609 | FIAX IGG TEST KIT | June 17, 1983 |
| K830669 | FIAX COMPLEMENT C4 TEST KIT | April 8, 1983 |
| K830668 | FIAX COMPLEMENT C3 TEST KIT | April 5, 1983 |
| K812968 | FIAX RHEUMATOID FACTOR TEST KIT | November 6, 1981 |
| K801642 | FIAX TEST KIT FOR THEOPHYLLINE QUANT. | August 27, 1980 |