Medical Device Recalls
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1 result found
510(K) Number: K970546 |
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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 Healthcare ADVIA Centaur Digitoxin (DGTN) 250 Test 09046419 50 Test ... | 2 | 12/11/2012 | Siemens Healthcare Diagnostics, Inc |
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