510(k) K921201 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
VITAL-PORT M.R.I. DUAL LUMEN VASCULAR ACCESS SYST.
| Applicant | Med Institute, Inc., West Lafayette IN, US |
| Decision | Substantially Equivalent, Jul 21, 1992 |
| Received | Mar 12, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921201
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.