510(k) K850967 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
STERILE CORMED MEDIPORT
| Applicant | Cormed, Inc., Sub. C.R.Bard, Inc., Medina NY, US |
| Decision | Substantially Equivalent, May 17, 1985 |
| Received | Mar 8, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850967
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.