510(k) K181077 ยท LEL Device, Sleep Assessment
ActiGraph CentrePoint Insight Watch
| Applicant | Actigraph, Pensacola FL, US |
| Decision | Substantially Equivalent, May 24, 2018 |
| Received | Apr 24, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K181077
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.