510(k) K893126 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
DESERET(R) INTRODUCER SET WITH VITACUFF(R) DEVICE
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Sandy UT, US |
| Decision | Unknown, Aug 10, 1989 |
| Received | Apr 25, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893126
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.