510(k) K083675 ยท NIE Catheter, Hemodialysis, Triple Lumen, Non-Implanted
POWER-TRIALYSIS TRIPLE LUMEN ACUTE DIALYSIS CATHETER
| Applicant | C.R. Bard, Inc., Salt Lake Ciy, UT, US |
| Decision | Substantially Equivalent, Mar 19, 2009 |
| Received | Dec 11, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083675
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.