Medical Device Recalls
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1 result found
510(K) Number: K921583 |
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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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BBL DrySlide PYR Kit, catalog number 231747 Product Usage: Presumptive diagnostic aid for group ... | 2 | 05/29/2013 | Becton Dickinson & Co. |
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