FDA 510(k) Application Details - K121287

Device Classification Name	Lift, Patient, Ac-Powered   More FDA Info for this Device
510(K) Number	K121287
Device Name	Lift, Patient, Ac-Powered
Applicant	D.T. DAVIS ENTERPRISES LTD. T/A HOVERTECH INT'L 513 SOUTH CLEWELL STREET BETHLEHEM, PA 18015 US Other 510(k) Applications for this Company
Contact	SUSAN PAVELKO Other 510(k) Applications for this Contact
Regulation Number	880.5500   More FDA Info for this Regulation Number
Classification Product Code	FNG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/30/2012
Decision Date	10/03/2012
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review