Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K132853 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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NovaPACS versions 8.4.7, 8.5.3, and 8.5.6. Distributed by Novarad Corporation. Picture archiving and... | 2 | 08/25/2016 | Novarad Corporation |
NovaPACS Diagnostic Viewer versions 8.3.7, 8.4.2, 8.4.3, and 8.4.4. Novarad Corporation | 2 | 05/06/2016 | Novarad Corporation |
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