510(k) K942784 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
NORFOLK OMEGA PORT-LP SUBCUTANEOUSLY IMPLANTED
| Applicant | Norfolk Medical Products, Inc., Skokie IL, US |
| Decision | Substantially Equivalent, May 2, 1995 |
| Received | Jun 14, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942784
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.