510(k) K840788 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
VASCULAR ACCESS PORT CHANGES IN MATER
| Applicant | Norfolk Medical Products, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Apr 24, 1984 |
| Received | Jan 6, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840788
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.