510(k) K963684 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
A2 PORT, DUAL LUMEN SYSTEM WITH DETACHED CATHETER, CATALOG # AP-01518 (MODIFIED)
| Applicant | Arrow Intl., Inc., Walpole MA, US |
| Decision | Substantially Equivalent, Oct 24, 1996 |
| Received | Aug 12, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963684
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.