510(k) K801632 ยท FIE Needle, Fistula
THE BELLCO FISTULA NEEDLES
| Applicant | Bellco Artifidial Organ Spec., Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 4, 1980 |
| Received | Jul 15, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801632
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.