Medical Device Recalls
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1 result found
510(K) Number: K143694 |
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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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Rhondium OVC3 One Visit Crown, Model FDI 24/25L USA 12/13L A2 HT, Nonsterile, Rx. The firm name on ... | 2 | 12/19/2019 | RHONDIUM LIMITED |
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