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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 30 Results
510(K) Number: K122958
 
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Product Description
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FDA Recall
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OSCOR ADELANTE BREEZEWAY 8F C55® S61CM D66CM Catalog # AB081040 Is designed to facilitate the intr... 2 12/19/2016 Oscor, Inc.
MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C55® S61CM D66CM GLOBALCatalog # 990061-055-000 Is... 2 12/19/2016 Oscor, Inc.
OSCOR ADELANTE BREEZEWAY 8F C90® S61CM D66CM Catalog # AB081042 Is designed to facilitate the intr... 2 12/19/2016 Oscor, Inc.
OSCOR ADELANTE BREEZEWAY 8F C120® S61CM D66CM Catalog # AB081043 Is designed to facilitate the in... 2 12/19/2016 Oscor, Inc.
OSCOR ADELANTE BREEZEWAY 8F C55® S79CM D84CM Catalog # AB081044 Is designed to facilitate the intr... 2 12/19/2016 Oscor, Inc.
OSCOR ADELANTE BREEZEWAY 8F C70® S79CM D84CM Catalog # AB081045 Is designed to facilitate the intr... 2 12/19/2016 Oscor, Inc.
OSCOR ADELANTE BREEZEWAY 8F C90® S79CM D84CM Catalog # AB081046 Is designed to facilitate the intro... 2 12/19/2016 Oscor, Inc.
OSCOR ADELANTE BREEZEWAY 8F C120® S79CM D84CM Catalog # AB081047 Is designed to facilitate the in... 2 12/19/2016 Oscor, Inc.
OSCOR ADELANTE BREEZEWAY 8F STRAIGHT S61CM D66CM Catalog # AB081210 Is designed to facilitate the... 2 12/19/2016 Oscor, Inc.
OSCOR ADELANTE BREEZWAY 8F STRAIGHT S79CM D84CM Catalog # AB081211 Is designed to facilitate the ... 2 12/19/2016 Oscor, Inc.
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