510(k) K890518 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
SINGLE LUMEN S.E.A.-PORT VASCULAR ACCESS SYSTEM
| Applicant | Harbor Medical Devices, Inc., Boston MA, US |
| Decision | Substantially Equivalent, Apr 21, 1989 |
| Received | Feb 2, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890518
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.