510(k) K142793 ยท KNT Tubes, Gastrointestinal (And Accessories)
AbbVie PEG
| Applicant | AbbVie , Inc., North Chicago IL, US |
| Decision | Unknown, Jan 14, 2015 |
| Received | Sep 26, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142793
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 27, 2017 | AbbVie Inc. AbbVie PEG, PEG Kit 20FR, FOR ENTERAL USE ONLY, STERILE, Rx Only. Terminated |
KNT | None listed |
| Apr 27, 2017 | AbbVie Inc. AbbVie PEG, PEG Kit 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only. Terminated |
KNT | None listed |
| Apr 27, 2017 | AbbVie Inc. AbbVie PEG, PEG Kit 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only. Terminated |
KNT | None listed |
| Nov 22, 2016 | AbbVie Inc. AbbVie PEG Kit 20 FR Terminated |
KNT | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.