Terumo Corporation
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) | K252295 | Ryurei | LOX | 2026-03-27 | View |
| 510(k) | K250700 | Pen Injector Needle 32.5 | FMI | 2025-11-21 | View |
| 510(k) | K250751 | DualView Catheter | DQO | 2025-07-17 | View |
| 510(k) | K240818 | R2P Radifocus Glidewire Advantage | DQX | 2024-11-26 | View |
| 510(k) | K240859 | Glidewire GT-R | DQX | 2024-08-21 | View |
| 510(k) | K190427 | Immucise | FMF | 2019-07-18 | View |
| 510(k) | K181369 | Immucise Intradermal Injection System | FMI | 2018-11-13 | View |
| 510(k) | K173799 | NaviCross 0.018 | DQY | 2018-03-29 | View |
| 510(k) | K170417 | Glidewire GT | DQX | 2017-09-15 | View |
| 510(k) | K130493 | CAPIOX RX05 HOLLOW FIBER OXYGENATOR/RESERVOIR | DTZ | 2013-03-13 | View |
| 510(k) | K130280 | CAPIOX FX HOLLOW FIBER OXYGENATOR W/ RESERVOIR | DTZ | 2013-03-13 | View |
| 510(k) | K122544 | TERUMO SURFLASH SAFETY I.V. CATHETER | FOZ | 2012-09-05 | View |
| 510(k) | K113335 | HEARTRAIL III GUIDING CATHETER | DQO | 2012-07-16 | View |
No matching devices.
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