In Vitro Diagnostics, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 15
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K896867 | THYROID STIMULATING HORMONE-EIA-XT | February 23, 1990 |
| K896866 | LUTEINIZING HORMONE-EIA-XT | February 13, 1990 |
| K896863 | DIGOXIN-EIA-XT | February 13, 1990 |
| K896865 | VITRO T4-EIA-XT | January 30, 1990 |
| K896925 | T UPTAKE ENZYME IMMUNOASSAY CRIMPED TUBE KIT | January 18, 1990 |
| K896864 | FOLLICLE STIMULATING HORMONE-EIA-XT | January 11, 1990 |
| K873832 | REAGENTS FOR USE ON CONTRAVES DC300, DC500, AL801 | November 23, 1987 |
| K871185 | LITHIUM INTERNAL STANDARD 1 MEQ/L #60085 | May 28, 1987 |
| K871183 | FLAME PHOTOMETER STANDARD #60082 140 NA/5K | May 28, 1987 |
| K871184 | FLAME PHOTOMETER STANDARD #60083 160 NA/8K | May 28, 1987 |
| K871182 | FLAME PHOTOMETER STANDARD #60081 120 NA/2K | May 28, 1987 |
| K871188 | LITHIUM INTERNAL STANDARD 1500 MEQ/L #60086 | May 28, 1987 |
| K871186 | CESIUM DILUENT 1.5 MMOL CS/L #60087 | May 28, 1987 |
| K871187 | LITHIUM INTERNAL STANDARD 3000 MEQ/L #60084 | May 28, 1987 |
| K853304 | 21 HEMATOLOGY REAGENTS | November 12, 1985 |