FDA 510(k) Application Details - K223533

Device Classification Name	Stroller, Adaptive   More FDA Info for this Device
510(K) Number	K223533
Device Name	Stroller, Adaptive
Applicant	Ki Mobility LLC 5201 Woodward Drive Stevens Point, WI 54481 US Other 510(k) Applications for this Company
Contact	Mark Murphy Other 510(k) Applications for this Contact
Regulation Number	890.3850   More FDA Info for this Regulation Number
Classification Product Code	LBE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/23/2022
Decision Date	08/31/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review