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Actigraph

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K231532ActiGraph LEAP activity monitor (ActiGraph LEAP)June 23, 2023
K181077ActiGraph CentrePoint Insight WatchMay 24, 2018
K080545ACTITRAINERJuly 24, 2008