510(k) K211410 ยท MSD Catheter, Hemodialysis, Implanted
GlidePath 13F Long-Term Hemodialysis Catheter
| Applicant | Bard Peripheral Vascular, Inc., Tempe AZ, US |
| Decision | Unknown, Jun 4, 2021 |
| Received | May 6, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K211410
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.