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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 16 Results
510(K) Number: K032930
 
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Product Description
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Ultraflex Esophageal Stent System. Uncovered - Distal Release - 18/23/7. Catalog Number M00513700. S... 2 06/25/2010 Boston Scientific Corporation
Ultraflex Esophageal Stent System. Covered - Large - Proximal Release - 23/28/12/9. Catalog Number M... 2 06/25/2010 Boston Scientific Corporation
Ultraflex Esophageal Stent System. Uncovered - Distal Release - 18/23/15. Catalog Number M00513720. ... 2 06/25/2010 Boston Scientific Corporation
Ultraflex Esophageal Stent System. Covered - Distal Release - 18/23/10/7. Catalog Number M00513730. ... 2 06/25/2010 Boston Scientific Corporation
Ultraflex Esophageal Stent System. Covered - Distal Release - 18/23/12/9. Catalog Number M00513740. ... 2 06/25/2010 Boston Scientific Corporation
Ultraflex Esophageal Stent System. Covered - Distal Release - 18/23/15/12. Catalog Number M00513750.... 2 06/25/2010 Boston Scientific Corporation
Ultraflex Esophageal Stent System. Uncovered - Proximal Release - 18/23/7. Catalog Number M00513800.... 2 06/25/2010 Boston Scientific Corporation
Ultraflex Esophageal Stent System. Uncovered - Proximal Release - 18/23/10. Catalog Number M00513810... 2 06/25/2010 Boston Scientific Corporation
Ultraflex Esophageal Stent System. Uncovered - Proximal Release - 18/23/15. Catalog Number M00513830... 2 06/25/2010 Boston Scientific Corporation
Ultraflex Esophageal Stent System. Covered - Proximal Release - 18/23/10/7. Catalog Number M00513840... 2 06/25/2010 Boston Scientific Corporation
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