510(k) K832999 ยท FLS Monitor, Apnea, Facility Use
RESPIRATION MONITOR
| Applicant | Litton Medical Electronics, Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 13, 1984 |
| Received | Aug 18, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832999
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.