510(k) K915482 ยท DWD Suction Control, Intracardiac, Cardiopulmonary Bypass
B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PT
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Jan 7, 1992 |
| Received | Dec 6, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915482
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.