510(k) K981969 ยท LEL Device, Sleep Assessment
ULTIMA BODY POSITION SENSOR
| Applicant | Braebon Medical Corp., Kanata, CA |
| Decision | Substantially Equivalent, Aug 20, 1998 |
| Received | Jun 4, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981969
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.