Terumo Medical Corporation
FDA 510(k) & PMA Approved Devices — 10 products
Total Devices10
Categories5
Latest Approval2023-09-26
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| PMA | P210017 | Device, hemostasis, vascular | MGB | 2023-09-26 | View |
| 510(k) | K231044 | R2P Navicross | DQY | 2023-07-27 | View |
| 510(k) | K213531 | TR BAND Radial Compression Device | DXC | 2021-12-20 | View |
| 510(k) | K193125 | R2P Destination Slender Guiding Sheath | DYB | 2020-01-06 | View |
| 510(k) | K181237 | Glidesheath Slender Tibial Pedal Kit | DYB | 2018-08-03 | View |
| 510(k) | K173831 | Glidesheath Slender | DYB | 2018-05-08 | View |
| 510(k) | K172995 | Destination Carotid Guiding Sheath, Destination Peripheral Guiding Sheath, Destination Renal Guiding Sheath | DYB | 2017-11-21 | View |
| 510(k) | K171491 | R2P Destination Slender Guiding Sheath | DYB | 2017-10-05 | View |
| PMA | P140002 | STENT, SUPERFICIAL FEMORAL ARTERY | NIP | 2016-10-18 | View |
| PMA | P930038 | Device, hemostasis, vascular | MGB | 2016-05-12 | View |
No matching devices.