Medical Device Recalls
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1 result found
510(K) Number: K152977 |
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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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Ambra PACS UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R Software Version Number: V3.16.13.0 In... | 2 | 01/18/2017 | DICOM GRID INC |
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