Medical Device Recalls
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1 result found
510(K) Number: K813015 |
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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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Helioseal Clear Refill 1 x 1.25 g, REF/Product Code/Art. No. 558521AN and Helioseal Clear Assortmen... | 2 | 02/29/2016 | Ivoclar Vivadent, Inc. |
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