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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
510(K) Number: K073100
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Product Description
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FDA Recall
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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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