FDA 510(k) Application Details - K111739

Device Classification Name	Wheelchair, Mechanical   More FDA Info for this Device
510(K) Number	K111739
Device Name	Wheelchair, Mechanical
Applicant	PRIDE MOBILITY PRODUCTS CORP. 182 SUSQUEHANNA AVE. EXETER, PA 18643 US Other 510(k) Applications for this Company
Contact	KIMBERLY BLAKE Other 510(k) Applications for this Contact
Regulation Number	890.3850   More FDA Info for this Regulation Number
Classification Product Code	IOR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/21/2011
Decision Date	08/12/2011
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review