Medical Device Recalls
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1 result found
510(K) Number: K014027 |
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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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| OptiBond Solo Plus Self-Etch Adhesive System, Part Number 31966 | 2 | 09/23/2006 |
FEI # 2024312 Kerr Corp |
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