510(k) K791183 ยท LDF Electrode, Pacemaker, Temporary
SWAN-GANZ FLOW-DIRECTED CATHETER
| Applicant | Edwards Lifesciences, LLC, Irvine CA, US |
| Decision | Substantially Equivalent, Jul 12, 1979 |
| Received | Jun 25, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791183
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.