510(k) K832136 ยท FIE Needle, Fistula
DUAL FLOW NEEDLE
| Applicant | Travenol Laboratories, S.A., Walker MI, US |
| Decision | Substantially Equivalent, Oct 14, 1983 |
| Received | Jul 1, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832136
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.