Felton International, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K041280 | HUMAN SUBCUTANEOUS INJECTOR, MODEL HSI 500 | KZE | 2004-06-24 | View |
| 510(k) | K013256 | BI-3M NEEDLE-FREE INJECTOR SYSTEM | KZE | 2001-12-07 | View |
No matching devices.
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