Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K110413 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Power Processor 3K, 3K High Speed Stockyards Module Nameplate: PP 3K Stockyard (Refrig) 9707 REF A8... | 2 | 10/14/2021 |
FEI # 2050012 Beckman Coulter Inc. |
| Power Processor 1K Stockyard. The Power Processor performs all pre-analytical sample tube prepar... | 2 | 10/24/2017 |
FEI # 2050012 Beckman Coulter Inc. |
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