FDA 510(k) Application Details - K100843

Device Classification Name	Thermometer, Electronic, Clinical   More FDA Info for this Device
510(K) Number	K100843
Device Name	Thermometer, Electronic, Clinical
Applicant	BRAIN TUNNELGENIX TECHNOLOGIES CORP 8870 RAVELLO CT NAPLES, FL 34114 US Other 510(k) Applications for this Company
Contact	DANIEL KAMM Other 510(k) Applications for this Contact
Regulation Number	880.2910   More FDA Info for this Regulation Number
Classification Product Code	FLL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/25/2010
Decision Date	08/17/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review