Medical Device Recalls
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1 result found
510(K) Number: K021792 |
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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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| Integra Bilayer Matrix Wound Dressing, 8 in X 10 in (20 cm x 25 cm); Non-pyrogenic, Do not Re steril... | 2 | 04/07/2009 |
FEI # 3003418325 Integra LifeSciences Corp. |
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