510(k) K970442 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
TARGET VITAL-PORT VASCULAR ACCESS SYSTEM
| Applicant | Med Institute, Inc., West Lafayette IN, US |
| Decision | Substantially Equivalent, Apr 30, 1997 |
| Received | Feb 5, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970442
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.