510(k) K792305 ยท LEL Device, Sleep Assessment
A SLEEP ASSESSMENT DEVICE
| Applicant | Farrall Instruments, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 20, 1979 |
| Received | Nov 16, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792305
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.