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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 10 Results
510(K) Number: K951091
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Bronchial One Lumen Tube - Right 2 08/18/2015 Teleflex, Inc.
Bronchial Double Lumen Tube Set (Left), Sterile 2 08/18/2015 Teleflex, Inc.
Bronchial Double Lumen Tube Set (Right), Sterile 2 08/18/2015 Teleflex, Inc.
Bronchial One Lumen Tube - Left 2 08/18/2015 Teleflex, Inc.
Bronchial Double Lumen Tube Set (Left), Extra Length, Sterile 2 08/18/2015 Teleflex, Inc.
Carlens Bronchial Double Lumen Tube Set (Left) Sterile 2 08/18/2015 Teleflex, Inc.
Tracheopart Set (Left), Sterile 2 08/18/2015 Teleflex, Inc.
Tracheopart Set (Right), Sterile 2 08/18/2015 Teleflex, Inc.
White Bronchial Double Lumen Tube Set (Right) Sterile 2 08/18/2015 Teleflex, Inc.
Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube set is indicated for uses... 2 03/19/2014 Teleflex Medical
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