FDA 510(k) Application Details - K963817

Device Classification Name	Wheelchair, Standup   More FDA Info for this Device
510(K) Number	K963817
Device Name	Wheelchair, Standup
Applicant	LEVO USA BLEICHEWEG 5 DOTTIKON CH-5605 CH Other 510(k) Applications for this Company
Contact	THOMAS RAEBER Other 510(k) Applications for this Contact
Regulation Number	890.3900   More FDA Info for this Regulation Number
Classification Product Code	IPL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/23/1996
Decision Date	12/23/1997
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