J. L. Shepherd and Assoc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K915767 | MODEL 143 SERIES BLOOD PRODUCT IRRADIATORS | July 12, 1995 |
| K915766 | MODEL 109 SERIES BLOOD PRODUCTS IRRADIATORS | July 12, 1995 |