Medical Device Recalls
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1 result found
510(K) Number: K001172 |
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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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Product is an EO Sterile, Polyester braided and coated nonabsorbable surgical suture with double nee... | 2 | 05/24/2007 | C P Medical |
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