510(k) K123943 ยท MSD Catheter, Hemodialysis, Implanted
AMECATH DUAL LUMEN HEMODIALYSIS CATHETER
| Applicant | Ameco Medical Industries, Monroe CT, US |
| Decision | Substantially Equivalent, Apr 2, 2013 |
| Received | Dec 20, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123943
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.