510(k) K882448 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
MULTILUMEN CENTRAL VENOUS CATH. W/VITACUFF DEVICE
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Sandy UT, US |
| Decision | Substantially Equivalent, Aug 9, 1988 |
| Received | Jun 14, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882448
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.