FDA 510(k) Application Details - K982724

Device Classification Name	Wheelchair, Powered   More FDA Info for this Device
510(K) Number	K982724
Device Name	Wheelchair, Powered
Applicant	KURT MFG. CO. 1325 QUINCY ST. N.E. MINNEAPOLIS, MN 55413 US Other 510(k) Applications for this Company
Contact	PHIL SCHLANGEN Other 510(k) Applications for this Contact
Regulation Number	890.3860   More FDA Info for this Regulation Number
Classification Product Code	ITI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/05/1998
Decision Date	08/12/1999
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