Medical Device Recalls
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1 result found
510(K) Number: K932078 |
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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 F Sealant Refill 1 x 1.25 g, REF 558519AN, and Helioseal F Assortment (kit) 5 x 1.25 g, RE... | 2 | 11/04/2015 | Ivoclar A. G. |
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