510(k) K823433 ยท DYG Catheter, Flow Directed
BALLOON THERMODILUTION CATHETER #7164&
| Applicant | Critikon Company, LLC, Walker MI, US |
| Decision | Substantially Equivalent, Nov 30, 1982 |
| Received | Nov 16, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823433
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.