FDA 510(k) Application Details - K072882

Device Classification Name	Device, Vibration Threshold Measurement   More FDA Info for this Device
510(K) Number	K072882
Device Name	Device, Vibration Threshold Measurement
Applicant	OSACHI CO., LTD. 3027 E. SUNSET RD., SUITE 105 LAS VEGAS, NV 89120 US Other 510(k) Applications for this Company
Contact	JAMES R GREENWOOD Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LLN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/09/2007
Decision Date	01/08/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review