Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K121981 |
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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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ADVIA Centaur® iPTH ReadyPack Assay 500 Tests; REF 10492369, 10493615, 1049361. For in vitro diag... | 2 | 06/06/2013 | Siemens Healthcare Diagnostics, Inc |
ADVIA Centaur® iPTH ReadyPack Assay 100 Tests; REF 10492368. For in vitro diagnostic use in the q... | 2 | 06/06/2013 | Siemens Healthcare Diagnostics, Inc |
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