FDA 510(k) Applications Submitted by FELTON INTERNATIONAL, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K013256 | 10/01/2001 | BI-3M NEEDLE-FREE INJECTOR SYSTEM | FELTON INTERNATIONAL, INC. |
| K041280 | 05/13/2004 | HUMAN SUBCUTANEOUS INJECTOR, MODEL HSI 500 | FELTON INTERNATIONAL, INC. |
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