510(k) K180708 ยท PIF Gastrointestinal Tubes With Enteral Specific Connectors
Entuit LP Gastrostomy BR Low Profile Balloon Retention Feeding Tube, Entuit LP Gastrostomy BR Low Profile Balloon Retention Feeding Tube with ENFit Connection, Entuit LP Patient Care Kit, Entuit LP Patient Care Kit with ENFit Connection, PromaX Low Profile Gastrostomy Feeding Tube, PromaX LP Patie
| Applicant | Xeridiem Medical Devices, A Spectrum Plastics Group Company, Tucson AZ, US |
| Decision | Unknown, Oct 18, 2018 |
| Received | Mar 19, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180708
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.