Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K130253 |
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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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| Coulter PrepPlus 2, Part Number 378600, Product Usage: The COULTER PrepPlus 2, when used in com... | 2 | 07/07/2017 |
FEI # 2050012 Beckman Coulter Inc. |
| Coulter PrepPlus, Part Number 286600, Product Usage: The COULTER PrepPlus is a microprocessor-c... | 2 | 07/07/2017 |
FEI # 2050012 Beckman Coulter Inc. |
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