510(k) K803058 ยท LDF Electrode, Pacemaker, Temporary
SWAN-GANZ FLOW-DIRECTED MULTIPUR. CATH.
| Applicant | American Edwards Laboratories, Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 16, 1981 |
| Received | Dec 2, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K803058
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.