FDA 510(k) Application Details - K121561

Device Classification Name	Transport, Patient, Powered   More FDA Info for this Device
510(K) Number	K121561
Device Name	Transport, Patient, Powered
Applicant	THYSSENKRUPP ACCESSIBILITY B.V. VAN UTRECHTWEG 99 KRIMPEN AAN DEN IJSSEL ZUID-HOLLAND 2921 LN NL Other 510(k) Applications for this Company
Contact	ARNOLD HEIDEN Other 510(k) Applications for this Contact
Regulation Number	890.5150   More FDA Info for this Regulation Number
Classification Product Code	ILK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/29/2012
Decision Date	10/26/2012
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