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U.S. Department of Health and Human Services

Medical Device Recalls

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1 result found
510(K) Number: K905482
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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Deknatel Bondek® Plus Polyglycolic Absorbable Surgical Sutures, Bon+BG BR 3-0 DSL 19 1N (45cm), Tele... 2 08/26/2010 Telefelx Medical
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