FDA 510(k) Application Details - K090350

Device Classification Name	Wheelchair, Powered   More FDA Info for this Device
510(K) Number	K090350
Device Name	Wheelchair, Powered
Applicant	VESTIL MANUFACTURING CORP. 201 GROWTH PKWY. ANGOLA, IN 46703 US Other 510(k) Applications for this Company
Contact	RICK MICHAEL 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	02/11/2009
Decision Date	04/10/2009
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