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Actigraph, LLC

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K231532 ActiGraph LEAP activity monitor (ActiGraph LEAP)LEL2023-06-23 View
510(k) K080545 ACTITRAINERISD2008-07-24 View
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