Pharmacia Diagnostics, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K052793 | IMMUNOCAP/UNICAP GLIADIN IGA, IMMUNOCAP/UNICAP SPECIFIC IGA, MODELS 14-4425-40, 10-9306-02 | February 7, 2006 |
| K051218 | MODIFICATION TO: UNICAP SPECIFIC IGE | June 9, 2005 |
| K921011 | PHARMACIA CMV IGM ELISA | July 27, 1992 |
| K920702 | TOXOPLASMA GONDII (TOXO) IGM ENZYME-LINKED IMMUNO | July 8, 1992 |
| K915348 | EBV-VCA IGM ELISA | February 14, 1992 |
| K914022 | SERIOLOGICAL TEST KIT/IGM ANTIBODY VARI-ZOST VIRUS | January 27, 1992 |
| K912026 | DELFIA(R) 17 -OH-PROGESTERON KIT | June 25, 1991 |
| K902793 | RUBELLA IGG | July 31, 1990 |
| K902792 | TOXOPLASMA GONDII IGG | July 24, 1990 |