510(k) K802710 ยท FLS Monitor, Apnea, Facility Use
INFANT APNEA MONITOR
| Applicant | Douglas Scientific Products, Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 12, 1980 |
| Received | Oct 31, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802710
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.