510(k) K103220 ยท FKX System, Peritoneal, Automatic Delivery
VOYAGER PERITONEAL DIALYSIS SYSTEM
| Applicant | Deka Research & Development Corp., Manchester NH, US |
| Decision | Substantially Equivalent, Jul 29, 2011 |
| Received | Nov 1, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103220
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.