510(k) K863230 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
D200 ADVANCED COMPUTER CARDIAC ANALYSIS SYSTEM
| Applicant | Dextra Medical, Inc., Long Beach CA, US |
| Decision | Substantially Equivalent, Nov 25, 1986 |
| Received | Aug 21, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863230
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.