Hematology Marketing Assoc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K851843 | OSMOCEL 3 | July 30, 1985 |
| K851375 | TRI-COUNT | July 12, 1985 |
| K850096 | LASER-GLOBIN | March 29, 1985 |
| K850095 | LASER-DIL | March 29, 1985 |
| K850097 | LASER-LYSE | March 29, 1985 |
| K850094 | LASER-GLOBIN POWDER | March 29, 1985 |
| K844708 | TRI-COUNT CALIBRATOR | March 5, 1985 |
| K843485 | TRI-COUNT LASER | December 12, 1984 |
| K834371 | TRI-COUNT 10 | March 9, 1984 |
| K833130 | TRI-COUNT 7 | October 20, 1983 |
| K831306 | HEMACAL | June 16, 1983 |
| K830187 | FOCUS FLUID | March 1, 1983 |
| K830188 | OSMOCEL + | March 1, 1983 |
| K830186 | LYSIS + | February 28, 1983 |