Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K952199 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Active I-PTH ELISA, Part Number: DSL-10-8000 The DSL-10-80000 ACTIVE I-PTH Enzyme-Linked Immunosorb... | 2 | 12/09/2010 |
FEI # 2050012 Beckman Coulter Inc. |
| Active I-PTH Enzyme-Linked Immunosorbent Assay(ELISA), Part Number: DSL-10-8000 The DSL-10-8000 ACT... | 2 | 10/20/2010 |
FEI # 2050012 Beckman Coulter Inc. |
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