510(k) K891239 ยท KDL Set, Perfusion, Kidney, Disposable
MOP CATHETER
| Applicant | Bivona Medical Technologies, Gary IN, US |
| Decision | Substantially Equivalent, Nov 28, 1989 |
| Received | Mar 7, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891239
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.