510(k) K882190 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
S.E.A.-PORT(TM) VASCULAR ACCESS SYSTEM
| Applicant | Harbor Medical Devices, Inc., Boston MA, US |
| Decision | Substantially Equivalent, Jun 9, 1988 |
| Received | May 24, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882190
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.