Incore Co., Ltd.
FDA 510(k) & PMA Approved Devices — 6 products
Total Devices6
Categories6
Latest FDA decision2024-04-19
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K232216 | Hemoblock_S (Prescription); Hemoblock_S (OTC) | QSY | 2024-04-19 | View |
| 510(k) | K221054 | CORE-INJECTOR | FBK | 2022-12-21 | View |
| 510(k) | K220846 | CORE-SNARE | FDI | 2022-11-21 | View |
| 510(k) | K220081 | CORE-SPORT | OTJ | 2022-09-28 | View |
| 510(k) | K213338 | CORE-CLIP | PKL | 2022-06-23 | View |
| 510(k) | K211148 | CORE-Trocar | GCJ | 2022-06-21 | View |
No matching devices.