Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K222312 |
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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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| Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 13.0.0.1547, 13.1.0.... | 2 | 01/16/2026 | RAYSEARCH LABORATORIES AB |
| Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Num... | 2 | 02/19/2025 | RAYSEARCH LABORATORIES AB |
| RayStation 13.0.0.1547, 13.1.0.144 & 13.1.1.89. Radiation Therapy Treatment Planning System. | 2 | 05/01/2024 | RAYSEARCH LABORATORIES AB |
| RayStation 14.0.0.3338. Radiation Therapy Treatment Planning System. | 2 | 05/01/2024 | RAYSEARCH LABORATORIES AB |
| RayStation Software Version Numbers version numbers 8B, 9A, 9B, 10A, 10B, 11A, 11B, 12A, 12B, 2023B,... | 2 | 04/05/2024 | RAYSEARCH LABORATORIES AB |
| RayStation with the following product descriptions: 1. RayStation 12A, Software Version: 13.0.0.... | 2 | 09/02/2025 | RAYSEARCH LABORATORIES AB |
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