510(k) K002901 ยท MSD Catheter, Hemodialysis, Implanted
KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETER
| Applicant | The Kendall Company, Mansfield MA, US |
| Decision | Substantially Equivalent, Mar 28, 2001 |
| Received | Sep 18, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002901
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.