510(k) K090528 ยท MSD Catheter, Hemodialysis, Implanted
DUET LONG-TERM HEMODIALYSIS CATHETER SYSTEM, DUET LONG-TERM HEMODIALYSIS CATHETER SYSTEM CATHETER REPAIR KIT
| Applicant | C.R. Bard, Inc., Salt Lake Ciy, UT, US |
| Decision | Unknown, May 28, 2009 |
| Received | Feb 27, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090528
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.