510(k) K123630 ยท FKX System, Peritoneal, Automatic Delivery
FRESENIUS LIBERTY CYCLER
| Applicant | Fresenius Medical Care North America, Design Cente, Waltham MA, US |
| Decision | Substantially Equivalent, Sep 9, 2013 |
| Received | Nov 23, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123630
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 27, 2016 | Fresenius Medical Care Renal Therapies Group, LLC Fresenius Liberty Cycler-Peritoneal Dialysis Cycler
Model: 180111 and RTLR180111 Terminated |
FKX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.