FDA 510(k) Applications Submitted by ActiGraph, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K231532 | 05/26/2023 | ActiGraph LEAP activity monitor (ActiGraph LEAP) | ActiGraph, LLC |
| K080545 | 02/27/2008 | ACTITRAINER | ACTIGRAPH, LLC |
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