FDA 510(k) Application Details - K110788

Device Classification Name	Wheelchair, Mechanical   More FDA Info for this Device
510(K) Number	K110788
Device Name	Wheelchair, Mechanical
Applicant	COLUMBIA MEDICAL MANUFACTURING, LLC 11724 WILLAKE STREET SANTA FE SPRINGS, CA 90670 US Other 510(k) Applications for this Company
Contact	SUSAN JOHNSON 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	03/22/2011
Decision Date	05/06/2011
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review