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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: K030032
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Crosseal, fibrin sealant (human), This package***, One Applicator, Two Vial cups, Sterile, Disposabl... 3 09/30/2004 FEI # 3003183625
Omrix Biopharmaceuticals, Ltd. - Plasma Fract. Inst.
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