Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K132816 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Oncentra Brachy radiation therapy planning system software. | 2 | 12/15/2022 | Elekta, Inc. |
| Oncentra Brachy users using version 4.0 and above with Applicator Modeling license 170283-00 | 2 | 10/28/2021 | Elekta, Inc. |
| Oncentra Brachy 4.5 radiation therapy software The firm name on the label is Nucletron B.V. Once... | 2 | 10/26/2017 | Nucletron BV |
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