Mitsubishi Yuka America, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K915727 | ACTH IRMA KIT II MITSUBISHI YUKA | March 2, 1992 |
| K912536 | CALCITONIN KIT MITSUBISHI YUKA | July 18, 1991 |