Medical Device Recalls
-
|
1 to 6 of 6 Results
510(K) Number: K101491 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| UROSKOP Omnia. Model Number: 10094910 | 2 | 06/17/2025 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| UROSKOP Omnia Max. Model Number: 10762473 | 2 | 06/17/2025 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Uroskop Omnia, Model no. 10094910 - Product Usage: a solid state detector fluoroscopic X-ray system,... | 2 | 01/08/2021 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Uroskop Omnia -fluoroscopic X-ray system Model # 10094910 The Uroskop Omnia is a solid state det... | 2 | 03/07/2019 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| SIEMENS Uroskop Omnia Max ; a solid state detector fluoroscopic X-Ray system, primarily for urologic... | 2 | 05/23/2015 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Siemens Uroskop Omnia Max system The Uroskop Omnia is a solid state detector fluoroscopic X-Ray sy... | 2 | 10/02/2014 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
-







