Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K781846 |
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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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Arrow Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port for use with 7.5 F... | 2 | 08/25/2010 | Arrow International Inc |
Percutaneous Sheath Introducer (PSI) Kit with Integral Hemostasis Valve/Side Port for use with 7.5 -... | 2 | 05/05/2010 | Arrow International Inc |
Arrow Percutaneous Sheath Introducers | 2 | 06/24/2009 | Arrow International Inc |
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