510(k) K850369 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
QUINTON WHITE SEALING CAP
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Feb 15, 1985 |
| Received | Jan 31, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850369
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.