510(k) K901134 ยท KNT Tubes, Gastrointestinal (And Accessories)
ENTERA-FLO REPLACEMENT GASTROSTOMY TUBE
| Applicant | Fresenius Pharma, New Brunswick NJ, US |
| Decision | Unknown, Jun 20, 1990 |
| Received | Mar 12, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901134
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.