Actigraph

FDA Regulatory Profile

Actigraph appears in FDA public data with 0 recalls, 3 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 23, 2023.

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