Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K051650 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Siemens Acute Care CTNI TestPak-in vitro diagnostic test for the measurement of cardiac troponin I ... | 2 | 01/07/2016 | Siemens Healthcare Diagnostics Inc |
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