Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K123808 |
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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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Agility with Integrity R3.2 | 2 | 02/26/2018 | Elekta Limited |
Agility. Version 3.1 of the Integrity interface and control software for the Elekta range of medica... | 2 | 03/06/2014 | Elekta, Inc. |
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