Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K112613 |
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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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Integrity R1.2 | 2 | 02/26/2018 | Elekta Limited |
Integrity 1.1. Integrity is the interface and control software for the Elekta range of medical di... | 2 | 04/02/2014 | Elekta, Inc. |
Integrity. Version 1.1 of the Integrity interface and control software for the Elekta range of medi... | 2 | 03/06/2014 | Elekta, Inc. |
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