Gainor Medical Europe, Ltd.
FDA 510(k) & PMA Approved Devices — 13 products
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Total Devices13
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K926448 | I.V. ADMINISTRATION SET | FPA | 1994-05-02 | View |
| 510(k) | K931828 | CARELET SAFETY LANCET | FMK | 1993-10-15 | View |
| 510(k) | K931827 | CLEANLET, CLEANLET XL & KIDS | FMK | 1993-09-13 | View |
| 510(k) | K922441 | SURESEAL BANDAGE | KGX | 1993-08-10 | View |
| 510(k) | K913333 | I.V. PRIMING SET | FPA | 1991-10-23 | View |
| 510(k) | K902422 | NEEDLE, ASPIRATION & INJECTION, DISPOSABLE | FMI | 1991-06-06 | View |
| 510(k) | K902420 | CATHETER, NASAL, OXYGEN | CAT | 1991-04-17 | View |
| 510(k) | K902564 | NEEDLE, DIALYSIS | FIE | 1991-03-01 | View |
| 510(k) | K902426 | HEMODIALYSIS SYSTEM AND ACCESSORY | FJK | 1990-11-20 | View |
| 510(k) | K902421 | STOMACH, GASTRO-ENTEROSTOMY | KDH | 1990-11-20 | View |
| 510(k) | K902416 | SURELITE AND SURELITE XL BLOOD LANCET | FMK | 1990-08-01 | View |
| 510(k) | K902417 | BAG, URINE | KNX | 1990-07-16 | View |
| 510(k) | K900306 | HEMODIALYSIS BLOOD LINES | KOC | 1990-04-20 | View |
No matching devices.
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