FDA 510(k) Application Details - K000738

Device Classification Name	Wheelchair, Mechanical   More FDA Info for this Device
510(K) Number	K000738
Device Name	Wheelchair, Mechanical
Applicant	JACKSON COMPANY LLC. AIR CARGO COMPLEX BLDG. F AIR CARGO DRIVE SUITE 2100 BALTIMORE, MD 21240 US Other 510(k) Applications for this Company
Contact	DEBORAH WEIMAN 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	03/07/2000
Decision Date	05/26/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review