510(k) K243607 · FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
Moda-flx Hemodialysis System Cartridge (102121-001 )
| Applicant | Diality, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Dec 20, 2024 |
| Received | Nov 21, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K243607
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.