FDA 510(k) Application Details - K030829

Device Classification Name	Device, Vibration Threshold Measurement   More FDA Info for this Device
510(K) Number	K030829
Device Name	Device, Vibration Threshold Measurement
Applicant	XILAS MEDICAL, INC. 12665 SILICON DR. SAN ANTONIO, TX 78249 US Other 510(k) Applications for this Company
Contact	RUBEN G ZAMORANO 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	03/14/2003
Decision Date	12/05/2003
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