510(k) K802122 ยท FJI Dialyzer, Capillary, Hollow Fiber
CLIRANS TH13 HOLLOW FIBER DIALYZER
| Applicant | Terumo America, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 18, 1980 |
| Received | Sep 4, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802122
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.