Medical Device Recalls
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1 result found
510(K) Number: K000421 |
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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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| Biogel Skinsense N, Non-Latex, Powder-free Surgical Gloves with Biogel coating, Neoprene, Made from ... | 2 | 12/18/2002 |
FEI # 3002970705 SSL Americas Inc. |
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