Medical Device Recalls
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1 result found
510(K) Number: K072769 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| AngioJet Spiroflex Thrombectomy Set: Peripheral - UPN 106553-004, Catalog No.106553, Sterilized Usin... | 2 | 08/13/2015 | Boston Scientific Corporation |
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