510(k) K832324 ยท DYG Catheter, Flow Directed
THERMAL DILUTION CATHETER
| Applicant | Catheter Corp. of America, Walker MI, US |
| Decision | Substantially Equivalent, Nov 3, 1983 |
| Received | Jul 15, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832324
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.