510(k) K954879 ยท KNT Tubes, Gastrointestinal (And Accessories)
PERCUTANEOUS REPLACEMENT GASTROSTOMY FEEDING CATHETER TRAY (MODIFICATION)
| Applicant | United States Endoscopy Group, Inc., Mentor OH, US |
| Decision | Substantially Equivalent, Mar 29, 1996 |
| Received | Oct 13, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954879
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.