Medical Device Recalls
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1 result found
510(K) Number: K972034 |
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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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Ocular Conformer, Sterile, Porex Surgical Inc., 15 Dart Road, Newnan, GA 30265. The device is inten... | 3 | 09/20/2008 | Porex Surgical, Inc. |
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