510(k) K181175 ยท NIE Catheter, Hemodialysis, Triple Lumen, Non-Implanted
12F Tri-Flow Triple Lumen Catheter
| Applicant | Medical Components, Inc. (dba MedComp), Harleysville PA, US |
| Decision | Unknown, Jul 5, 2018 |
| Received | May 2, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181175
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.