510(k) K202150 ยท MSD Catheter, Hemodialysis, Implanted
GlidePath 7.5F Long-Term Dialysis Catheter
| Applicant | C.R. Bard, Inc., Tempe AZ, US |
| Decision | Unknown, Nov 18, 2020 |
| Received | Aug 3, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202150
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.