Kofu Factory of Terumo Corp.
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) | K123267 | SURFFLASH(R) PLUS SAFETY I.V. CATHETER | FOZ | 2012-11-02 | View |
| 510(k) | K052561 | TERUMO MICRO TAPERED PEN NEEDLE | FMI | 2005-11-23 | View |
No matching devices.
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