510(k) K862766 ยท LEL Device, Sleep Assessment
EPISON, ALERTING SYSTEM FOR EPILEPTICS
| Applicant | Zygo Industries, Inc., Portland OR, US |
| Decision | Substantially Equivalent, Mar 13, 1987 |
| Received | Jul 22, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862766
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.