510(k) K810177 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
PATIENT MONITOR MODEL CM130, 140
| Applicant | Honeywell, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 25, 1981 |
| Received | Jan 22, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810177
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.