510(k) K885221 ยท DQO Catheter, Intravascular, Diagnostic
MULTILUMEN CENTRAL VENOUS CATHETER
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Sandy UT, US |
| Decision | Substantially Equivalent, Dec 28, 1989 |
| Received | Dec 20, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885221
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.