510(k) K872838 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
NORFOLK NORPORT (TM) -SP (SKIN PARALLEL)
| Applicant | Norfolk Medical Products, Inc., Skokie IL, US |
| Decision | Substantially Equivalent, Aug 25, 1987 |
| Received | Jul 20, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872838
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.