510(k) K913786 ยท KNT Tubes, Gastrointestinal (And Accessories)
FLEXIFLO OVER-THE-GUIDEWIRE GAST KIT W/CR-BAR BUMP
| Applicant | Abbott Laboratories, Columbus OH, US |
| Decision | Unknown, Nov 5, 1991 |
| Received | Aug 23, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913786
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.