510(k) K894650 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
Q-PORT SYSTEM KIT
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Mar 12, 1990 |
| Received | Jul 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894650
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.