Medical Device Recalls
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11 to 13 of 13 Results
510(K) Number: K200569 |
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 Model Number: (9A)9.0.0.113, 9B (9.1.0.933), 9B Service pack (9.2.0.483), 10A (10.0.0.115... | 2 | 04/15/2021 |
FEI # 3007774465 RAYSEARCH LABORATORIES AB |
| RayStation 4, 4.5, 4.7, 4.9, 5, 6, 7, 8A, 8B, 9A, 9B, RayPlan 1, 2, 7, 8A, 8B, 9A, 9B, including all... | 2 | 12/15/2020 |
FEI # 3007774465 RAYSEARCH LABORATORIES AB |
| RayStation standalone software treatment planning system, Model No. 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.... | 2 | 11/20/2020 |
FEI # 3007774465 RAYSEARCH LABORATORIES AB |
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