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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K142793
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AbbVie PEG, PEG Kit 20FR, FOR ENTERAL USE ONLY, STERILE, Rx Only. 2 05/31/2017 FEI # 3009751352
AbbVie Inc.
AbbVie PEG, PEG Kit 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only. 2 05/31/2017 FEI # 3009751352
AbbVie Inc.
AbbVie PEG, PEG Kit 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only. 2 05/31/2017 FEI # 3009751352
AbbVie Inc.
AbbVie PEG Kit 20 FR 2 12/17/2016 FEI # 3009751352
AbbVie Inc.
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