Immuno-Products Industries
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K853122 | IMMUNO-PROD IND FLUORE TREPONE ANTIBODY ABSORPED | September 19, 1985 |
| K852230 | ANA/LITE-RL TEST SYSTEM | July 10, 1985 |
| K852231 | ANA/LITE-HEP-2 TEST SYSTEM | July 10, 1985 |
| K843613 | FLUORESCENT TREPONEMEL ANTIBODY-ABSORB | October 31, 1984 |
| K831054 | ANTINUCLEAR ANTIBODY TISSUE CULTURE SUB | April 27, 1983 |
| K830652 | ANTI N DNA-HCP | March 24, 1983 |
| K821576 | ANTINUCLEAR ANTIBODY SCREEN FLOURESC | June 10, 1982 |
| K810982 | ANTITHYROID ANTIBODY IMMUNOFLUORESCENT | May 1, 1981 |
| K810983 | ANTISMOOTH MUSCLE ANTIBODY TEST SYS | May 1, 1981 |
| K810985 | ANTINUCLEAR ANTIBODY IMMUNOFLUORESCENT | May 1, 1981 |
| K810984 | ANTIMITOCHONDRIAL IMMUNOFLUORESCENT TEST | May 1, 1981 |
| K810981 | ANTI NDNA IMMUNOFLOURESCENT TEST SYS | April 29, 1981 |