510(k) K981994 ยท MSD Catheter, Hemodialysis, Implanted
VASCATH OPTI-FLOW LONG TERM DUAL LUMEN HEMODIALYSIS CATHETER
| Applicant | C.R. Bard, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Sep 3, 1998 |
| Received | Jun 8, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981994
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.