510(k) K131814 ยท MSD Catheter, Hemodialysis, Implanted
AMECATH DUAL LUMEN IMPLANTED HEMODIALYSIS CATHETER
| Applicant | Ameco Medical Industries, Monroe CT, US |
| Decision | Unknown, Jul 26, 2013 |
| Received | Jun 20, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K131814
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.