Felton International, 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 |
|---|
| K041280 | HUMAN SUBCUTANEOUS INJECTOR, MODEL HSI 500 | June 24, 2004 |
| K013256 | BI-3M NEEDLE-FREE INJECTOR SYSTEM | December 7, 2001 |