Medical Device Recalls
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1 result found
510(K) Number: K113363 |
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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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AngioJet SOLENT Dista Thrombectomy Set: UPN 111303-001, Catalog No. 111303, Sterilized Using Ethylen... | 2 | 08/13/2015 | Boston Scientific Corporation |
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