510(k) K880297 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
SEA - PORT INFUSION SET
| Applicant | Harbor Medical Devices, Inc., Boston MA, US |
| Decision | Substantially Equivalent, Feb 19, 1988 |
| Received | Jan 25, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880297
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.