Medical Device Recalls
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1 result found
510(K) Number: K003871 |
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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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The Applied GelPort Hand Access Device consists of a GelSeal Cap, Wound retractor (base). Standard W... | 2 | 11/16/2005 | Applied Medical Resources Corp |
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