510(k) K961615 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
LOW PROFILE TITANIUM PORT DETACHED CATHETER SYSTEM CATALOG #1037
| Applicant | Arrow Intl., Inc., Walpole MA, US |
| Decision | Substantially Equivalent, Jul 19, 1996 |
| Received | Apr 26, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961615
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.