FDA 510(k) Application Details - K972486

Device Classification Name	Bed, Patient Rotation, Powered   More FDA Info for this Device
510(K) Number	K972486
Device Name	Bed, Patient Rotation, Powered
Applicant	SPAN-AMERICA MEDICAL SYSTEMS, INC. 70 COMMERCE DR. P.O. BOX 5231 GREENVILLE, SC 29615 US Other 510(k) Applications for this Company
Contact	WANDA TOTTON Other 510(k) Applications for this Contact
Regulation Number	890.5225   More FDA Info for this Regulation Number
Classification Product Code	IKZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/02/1997
Decision Date	02/20/1998
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