510(k) K833572 ยท DYG Catheter, Flow Directed
HEPARIN-COATED BALLOON THERMODILUT
| Applicant | Critikon Company, LLC, Walker MI, US |
| Decision | Substantially Equivalent, Jan 30, 1984 |
| Received | Oct 12, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833572
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.