510(k) K111651 ยท MSD Catheter, Hemodialysis, Implanted
SPLIT CATH III
| Applicant | Medical Components, Inc., Harleysville PA, US |
| Decision | Unknown, Dec 8, 2011 |
| Received | Jun 13, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111651
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 30, 2015 | Medical Components, Inc dba MedComp Medcomp Duo-Flow 400XL Catheter, Hemo-Flow Catheter, SLX Catheter, Triple Lumen Infusion Catheter, CT rated PICC, Split Cath III, PC Split Cath III;
AngioDynamics product- Dura-Flow Catheter, Schon Terminated |
MSD | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.