510(k) K923983 ยท KNT Tubes, Gastrointestinal (And Accessories)
PEG GUIDEWIRE SYSTEM GASTROSTOMY TUBE KIT
| Applicant | Sandoz Nutrition, Minneapolis MN, US |
| Decision | Substantially Equivalent, Apr 6, 1993 |
| Received | Aug 7, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923983
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.