510(k) K002210 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
SYNTRA DIALYZER, MODEL SYNTRA 120, 160
| Applicant | Baxter Healthcare Corp, Mcgaw Park IL, US |
| Decision | Substantially Equivalent, Feb 14, 2001 |
| Received | Jul 21, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002210
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.