510(k) K240359 · FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
PowerGlide Pro Midline Catheter
| Applicant | Becton, Dickinson and Company (Bard Access Systems, Inc.), Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jul 29, 2024 |
| Received | Feb 6, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240359
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.