Medical Device Recalls
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1 to 5 of 5 Results
Recall Date to: 08/27/2014 510(K) Number: K001139 |
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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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Biosense Webster PREFACE Guiding Sheath, Posterior, for the introduction of intravascular electrophy... | 2 | 02/28/2007 | Biosense Webster, Inc. |
Biosense Webster PREFACE Guiding Sheath, Multipurpose Short, for the introduction of intravascular e... | 2 | 02/28/2007 | Biosense Webster, Inc. |
Biosense Webster PREFACE Guiding Sheath, Multipurpose 77cm, for the introduction of intravascular el... | 2 | 02/28/2007 | Biosense Webster, Inc. |
Biosense Webster PREFACE Guiding Sheath, Multipurpose 62cm, for the introduction of intravascular el... | 2 | 02/28/2007 | Biosense Webster, Inc. |
Biosense Webster PREFACE Guiding Sheath, Anterior, for the introduction of intravascular electrophys... | 2 | 02/28/2007 | Biosense Webster, Inc. |
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