FDA 510(k) Application Details - K130864

Device Classification Name	Transport, Patient, Powered   More FDA Info for this Device
510(K) Number	K130864
Device Name	Transport, Patient, Powered
Applicant	AAT ALBER ANTRIEBSTECHNIK GMBH 2611 SHARK CIRCLE TEXAS CITY, TX 77591 US Other 510(k) Applications for this Company
Contact	STEFANIE D BANKSTON 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	03/28/2013
Decision Date	02/06/2014
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