510(k) K884322 ยท LFJ Catheter, Subclavian
SUBCLAVIAN HEMODIALYSIS CATHETER
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Sandy UT, US |
| Decision | Substantially Equivalent, Apr 25, 1989 |
| Received | Oct 14, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884322
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.