510(k) K203575 ยท MSD Catheter, Hemodialysis, Implanted
GlidePath Retro Long-Term Hemodialysis Catheter
| Applicant | C.R. Bard, Inc., Tempe AZ, US |
| Decision | Unknown, Jul 1, 2021 |
| Received | Dec 7, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203575
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.