Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K061566 |
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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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ev3" sterile EO, single Use, Visi-Pro Balloon-Expandable Biliary Stent System. Model Numbers: P... | 2 | 09/26/2008 | Ev3, Inc |
ev3" 55442-2920, sterile EO, single Use, Visi-Pro Balloon-Expandable Peripheral Stent System. Mode... | 2 | 09/26/2008 | Ev3, Inc |
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