Felton International, Inc. · Class II · Cleared Dec 7, 2001
| K-number | K013256 |
| Device name | BI-3M NEEDLE-FREE INJECTOR SYSTEM |
| Applicant | Felton International, Inc. |
| Product code | KZE |
| Device class | Class II |
| Decision date | Dec 7, 2001 |
| Decision | Substantially Equivalent |
| Regulation | 880.5430 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov