510(k) K870260 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
HICKMAN TITANIUM SUBCUTANEOUS PORT
| Applicant | C.R. Bard, Inc., Murray Hill NJ, US |
| Decision | Substantially Equivalent, Apr 15, 1987 |
| Received | Jan 23, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870260
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.