510(k) K903440 ยท FIE Needle, Fistula
VIVAMED FISTULA NEEDLE
| Applicant | S.S. Ent., Weston CT, US |
| Decision | Substantially Equivalent, Apr 20, 1992 |
| Received | Jul 31, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903440
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.