Denka Seiken'S
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Known Names
denka seiken, denka seiken co
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K011400 | MRSA-SCREEN | March 27, 2002 |
| K013359 | LP(A)-LATEX SEIKEN ASSAY KIT | March 8, 2002 |
| K011958 | CRP-LATEX (II) SEIKEN HIGH SENSITIVITY ASSAY KIT | December 4, 2001 |
| K981734 | VTEC-RPLA SEIKEN | September 22, 1998 |