FDA 510(k) Application Details - K092675

Device Classification Name	Device, Biofeedback   More FDA Info for this Device
510(K) Number	K092675
Device Name	Device, Biofeedback
Applicant	MEDOTECH A/S 13417 QUIVAS ST WESTMINSTER, CO 80234 US Other 510(k) Applications for this Company
Contact	Calley Herzog Other 510(k) Applications for this Contact
Regulation Number	882.5050   More FDA Info for this Regulation Number
Classification Product Code	HCC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/01/2009
Decision Date	03/03/2010
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