FDA 510(k) Application Details - K041503

Device Classification Name	Lift, Patient, Ac-Powered   More FDA Info for this Device
510(K) Number	K041503
Device Name	Lift, Patient, Ac-Powered
Applicant	D.T. DAVIS ENTERPRISES LTD. 513 S. CLEWELL ST. BETHLEHEM, PA 18015-4537 US Other 510(k) Applications for this Company
Contact	DAVID T DAVIS 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	06/07/2004
Decision Date	08/12/2004
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