510(k) K873735 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
MEDTRONIC CATHETER ACCESS PORT MODEL 8500
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Nov 3, 1987 |
| Received | Sep 15, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873735
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.