510(k) K122400 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
CARDIOX FLOW DETECTION SYSTEM
| Applicant | Cardiox Corp., Columbus OH, US |
| Decision | Substantially Equivalent, Nov 5, 2013 |
| Received | Aug 7, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122400
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.