FDA 510(k) Application Details - K954671

Device Classification Name	Bed, Patient Rotation, Powered   More FDA Info for this Device
510(K) Number	K954671
Device Name	Bed, Patient Rotation, Powered
Applicant	PROBED MEDICAL TECHNOLOGIES, INC. 44325 YALE RD. WEST CHILLIWACK, B.C. V2R 4H2 CA Other 510(k) Applications for this Company
Contact	STEVE PLUMMER 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	10/10/1995
Decision Date	04/01/1996
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