Medical Device Recalls
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1 result found
510(K) Number: K970330 |
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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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QuikLYTE Dilution Check: used to monitor and adjust for the dilution ratio on Dimension clinical ch... | 2 | 04/07/2015 | Siemens Healthcare Diagnostics, Inc. |
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