510(k) K800164 ยท FLS Monitor, Apnea, Facility Use
413A NEONATAL MONITOR
| Applicant | Xerox Corp., Walker MI, US |
| Decision | Substantially Equivalent, Apr 10, 1980 |
| Received | Jan 25, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800164
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.