510(k) K231532 ยท LEL Device, Sleep Assessment
ActiGraph LEAP activity monitor (ActiGraph LEAP)
| Applicant | Actigraph, LLC, Pensacola FL, US |
| Decision | Substantially Equivalent, Jun 23, 2023 |
| Received | May 26, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K231532
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.