510(k) K200891 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
BD Intima II Closed IV Catheter System, BD Intima II PLUS Closed IV Catheter System
| Applicant | Becton, Dickinson and Company, Sandy UT, US |
| Decision | Substantially Equivalent, Jun 2, 2021 |
| Received | Apr 3, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200891
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.