Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K220141 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| RayStation 11B | 2 | 06/28/2022 |
FEI # 3007774465 RAYSEARCH LABORATORIES AB |
| RayStation 12.0.0.932, 12.1.0.1221, 12.0.3.68, 12.0.4.12 &12.3.0.119. Radiation Therapy Treatment Pl... | 2 | 05/01/2024 |
FEI # 3007774465 RAYSEARCH LABORATORIES AB |
| Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Num... | 2 | 02/19/2025 |
FEI # 3007774465 RAYSEARCH LABORATORIES AB |
| RayStation with the following product descriptions: 1. RayStation 11B, Software Version: 12.0.0.... | 2 | 09/02/2025 |
FEI # 3007774465 RAYSEARCH LABORATORIES AB |
| RayStation/RayPlan. Model/Catalog Numbers: 12.0.0, 12.1.0, 12.0.3, 12.0.4, 12.3.0. Software Versio... | 2 | 01/16/2026 |
FEI # 3007774465 RAYSEARCH LABORATORIES AB |
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