510(k) K833918 ยท DYG Catheter, Flow Directed
INFUSION PORT BALLOON THERMODILUTION
| Applicant | Critikon Company, LLC, Walker MI, US |
| Decision | Substantially Equivalent, Jan 30, 1984 |
| Received | Nov 14, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833918
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.