Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K073100 |
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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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8F Safe Sheath Introducer, Catalog number: V18; AngioDynamics, INC. The Valved Introducer sheat... | 2 | 10/13/2011 | Angiodynamics, INC |
Oscor Adelante Luer-Lock Peel Away Introducer Set, for introduction of diagnostic or therapeutic dev... | 2 | 10/29/2008 | Oscor, Inc. |
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