510(k) K895030 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
LIFE-LINE(TM) VASCULAR ACCESS SYSTEM
| Applicant | Medical Engineering and Development Institute, West Lafayette IN, US |
| Decision | Unknown, Apr 17, 1990 |
| Received | Aug 8, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895030
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.