510(k) K924125 ยท DXX System, Catheter Control, Steerable
CRI ELECTRONIC CONTROL SYSTEM
| Applicant | Catheter Research C/O Burditt, Bowles & Radzius, Indianapolis IN, US |
| Decision | Substantially Equivalent, May 26, 1993 |
| Received | Aug 17, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924125
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.