Medical Device Recalls
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1 result found
510(K) Number: K130924 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BruxZir Shaded, Model No. 70-1167-NOW0001, 70-1167-NOW0002, 70-1167-NOW0003, 70-1167-NOW0005, 70-116... | 2 | 09/27/2016 |
FEI # 3011649314 Prismatik Dentalcraft, Inc |
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