FDA 510(k), K231337, EndeavorRx

FDA 510(k), K231337, EndeavorRx

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510(K) Number: K231337
Device Name: EndeavorRx
Manufacturer: Bhupinder Singh
Device Classification Name: Digital Therapeutic Software For Attention Deficit Hyperactivity Disorder
Regulation Number: QFT
Classification Product Code: KXA
Date Received: 05/08/2023
Decision Date: 12/13/2023
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
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