Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K932955 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ADVIA Centaur Progesterone; Catalog Number: 10310305 10315522 10333111 Product Usage: The PROG m... | 2 | 03/09/2017 |
FEI # 1219913 Siemens Healthcare Diagnostics, Inc |
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