510(k) K890277 ยท DYB Introducer, Catheter
HEMOSTASIS VALVE, WITH OR WITHOUT SIDE PORT
| Applicant | Oscor Medical Corp., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Mar 10, 1989 |
| Received | Jan 18, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890277
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.