510(k) K183219 ยท NIE Catheter, Hemodialysis, Triple Lumen, Non-Implanted
Trio-CT Triple Lumen Catheter
| Applicant | Medical Components, Inc. (dba MedComp), Harleysville PA, US |
| Decision | Unknown, Jun 14, 2019 |
| Received | Nov 20, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183219
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.