510(k) K891764 ยท LFK Catheter, Femoral
FC-101 FEMORAL CATHETER GUIDE WIRE
| Applicant | Akcess Medical Products, Inc., New Brunswick NJ, US |
| Decision | Substantially Equivalent, Apr 7, 1989 |
| Received | Mar 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891764
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.