K-number	K231532
Device name	ActiGraph LEAP activity monitor (ActiGraph LEAP)
Applicant	Actigraph, LLC
Product code	LEL
Device class	Class II
Decision date	Jun 23, 2023
Decision	Substantially Equivalent
Regulation	882.5050

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Source

View the full FDA submission: accessdata.fda.gov

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ActiGraph LEAP activity monitor (ActiGraph LEAP)

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