Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K071834 |
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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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Siemens Acute Care pBNP TestPak- in vitro diagnostic test for the quantitative measurement of N-term... | 2 | 01/07/2016 | Siemens Healthcare Diagnostics Inc |
Stratus(R) CS Acute care(TM) NT - proBNP TestPak reagent (CPBNPM) The Stratus(R) CS Acute care(T... | 2 | 05/10/2012 | Siemens Healthcare Diagnostics, Inc. |
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