Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K081281 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Oncentra Brachy radiation therapy planning software designed to analyze and plan radiation treatment... | 2 | 06/04/2015 | Elekta, Inc. |
Oncentra External Beam 4.1. Radiation treatment planning software designed to analyze and plan ra... | 2 | 10/23/2012 | Elekta, Inc. |
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