Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K060698 |
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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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Breeze Self-Adhesive Resin Cement, part number: N97F. The intended use is for cementation of porcela... | 2 | 02/24/2012 | Kerr Corporation |
Breeze Self-Adhesive Resin Cement, Part Number: N97A, Product Usage: The intended use of this ... | 2 | 11/14/2011 | Kerr/pentron Dba Kerr Corporation And Pentron Clinical |
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