Akers Laboratories, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K040293 | HEALTHTEST HEPARIN/PLATELET FACTOR 4 ANTIBODY ASSAY | May 28, 2004 |
| K031579 | INSTAREAD LITHIUM SYSTEM | December 19, 2003 |
| K030815 | AKERS LABORATORIES INC. BLOOD CELL SEPARATOR | September 17, 2003 |