510(k) K770179 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
CARDIAC CATHETERIZATION LAB MONITOR SYS
| Applicant | General Electric Co., Walker MI, US |
| Decision | Substantially Equivalent, Apr 5, 1977 |
| Received | Jan 27, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770179
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.