FDA 510(k) Application Details - K072256

Device Classification Name	More FDA Info for this Device
510(K) Number	K072256
Device Name	HF54 COMBINATION ULTRASOUND INTERFERENTIAL AND PREMODULATED STIMULATION SYSTEM WITH OPTIONAL HANDS-FREE OPERATION, MODEL
Applicant	HILL LABORATORIES CO. 3 N. BACTON HILL RD. FRAZER, PA 19355 US Other 510(k) Applications for this Company
Contact	BRADY ALLER Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PFW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/13/2007
Decision Date	03/12/2008
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