Medical Device Recalls
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1 result found
510(K) Number: K192376 |
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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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MOL3655 Simplexa VZV Swab Direct - Product Usage: is intended for use on the LIAISON MDX instrument ... | 2 | 07/10/2020 | DiaSorin Molecular LLC |
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