510(k) K093927 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
6F TRIPLE LUMEN POWERLINE CENTRAL VENOUS CATHETER, 5F DUAL LUMEN POWERLINE CENTRAL VENOUS CATHETER
| Applicant | C.R. Bard, Inc., Salt Lake Ciy, UT, US |
| Decision | Substantially Equivalent, Feb 4, 2010 |
| Received | Dec 22, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093927
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.