Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K111945 |
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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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IMPAX RIS QDOC 5.8 | 2 | 02/03/2014 | AGFA Corp. |
Enterprise Imaging Desktops Enterprise Imaging Desktops (Radiology Suite/Cardiology Suite) when d... | 2 | 10/11/2018 | Agfa Healthcare NV |
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