510(k) K860449 ยท FIE Needle, Fistula
MODIFICATION TOP ULTRA THINWALL A-V FISTULA NEEDLE
| Applicant | Top Corp., Littleton CO, US |
| Decision | Substantially Equivalent, Feb 26, 1986 |
| Received | Feb 4, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860449
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.