510(k) K122952 ยท FJI Dialyzer, Capillary, Hollow Fiber
NIPRO PUREFLUX-L HEMODIALYZER
| Applicant | Nipro Medical Corporation, Suwanee GA, US |
| Decision | Substantially Equivalent, Dec 4, 2013 |
| Received | Sep 25, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122952
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.