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ActiGraph LEAP activity monitor (ActiGraph LEAP)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231532
510(k) Type
Special
Applicant
ActiGraph, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2023
Days to Decision
28 days
Submission Type
Summary

ActiGraph LEAP activity monitor (ActiGraph LEAP)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231532
510(k) Type
Special
Applicant
ActiGraph, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2023
Days to Decision
28 days
Submission Type
Summary