Medical Device Recalls
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1 result found
510(K) Number: K032342 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Coulter LH 750, Coulter LH 780, and Coulter LH 500 Analyzers Hematology Analyzers are quantitative,... | 2 | 09/07/2017 | Beckman Coulter Inc. |
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