510(k) K994111 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
CELSITE, MODELS ST401L, ST405L
| Applicant | B. Braun/Mcgaw, Allentown PA, US |
| Decision | Substantially Equivalent, Jan 3, 2000 |
| Received | Dec 6, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K994111
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.