510(k) K123292 ยท NIE Catheter, Hemodialysis, Triple Lumen, Non-Implanted
T3
| Applicant | Medcomp, Harleysville PA, US |
| Decision | Substantially Equivalent, Jun 11, 2013 |
| Received | Oct 22, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123292
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.