510(k) K180605 ยท KNT Tubes, Gastrointestinal (And Accessories)
GastroFlush
| Applicant | Bionix Development Corporation, Toledo OH, US |
| Decision | Substantially Equivalent, Oct 24, 2018 |
| Received | Mar 7, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180605
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.