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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 5 of 5 Results
Date Classified to: 06/19/2014 510(K) Number: K001139
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Product Description
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Recall
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Biosense Webster PREFACE Guiding Sheath, Anterior, for the introduction of intravascular electrophys... 2 Feb-28-2007 Biosense Webster, Inc.
Biosense Webster PREFACE Guiding Sheath, Multipurpose 62cm, for the introduction of intravascular el... 2 Feb-28-2007 Biosense Webster, Inc.
Biosense Webster PREFACE Guiding Sheath, Multipurpose 77cm, for the introduction of intravascular el... 2 Feb-28-2007 Biosense Webster, Inc.
Biosense Webster PREFACE Guiding Sheath, Multipurpose Short, for the introduction of intravascular e... 2 Feb-28-2007 Biosense Webster, Inc.
Biosense Webster PREFACE Guiding Sheath, Posterior, for the introduction of intravascular electrophy... 2 Feb-28-2007 Biosense Webster, Inc.
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