Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K955157 |
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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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| ProSpecT Giardia/Cryptosporidium Microplate Assay. Catalog #: 2458496. | 3 | 08/17/2004 |
FEI # 1924669 Remel, Inc. |
| ProSpecT Giardia/Cryptosporidium Micorplate Assay. Catalog #: 2458496. | 3 | 08/17/2004 |
FEI # 1924669 Remel, Inc. |
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