510(k) K792081 ยท DSI Detector And Alarm, Arrhythmia
SPECTRA CENTRAL PT MONITORING SYS
| Applicant | American Optical Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 13, 1979 |
| Received | Oct 16, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792081
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.