Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K963806 |
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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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Tunneled Central Venous Catheters With PASV Valve Technology And Polyester Cuff - PASV CVC/TL/10/IK ... | 2 | 09/02/2005 | Boston Scientific Corporation |
PASV Central Venous Catheter, 7F, Cat. # CVC702IK, Model # M0001CVC702IK. The 7Fr PASV Central Ven... | 3 | 08/10/2005 | Boston Scientific Corporation |
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