Medical Device Recalls
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1 result found
510(K) Number: K961458 |
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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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9180 Electrolyte Analyzer - Product Usage: intended to be used for the measurement of sodium, potass... | 2 | 02/08/2021 | Roche Diagnostics Operations, Inc. |
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