510(k) K904785 ยท DRA Catheter, Steerable
CRI CYNOSAR CATHETER
| Applicant | Catheter Research C/O Burditt, Bowles & Radzius, Indianapolis IN, US |
| Decision | Substantially Equivalent, Mar 6, 1991 |
| Received | Oct 22, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904785
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.