510(k) K172204 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
BD Intima II PLUS Closed IV Catheter System
| Applicant | Becton, Dickinson and Company, Sandy UT, US |
| Decision | Substantially Equivalent, Aug 17, 2017 |
| Received | Jul 21, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172204
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.