FDA 510(k) Application Details - K090766

Device Classification Name	Devices, Breath Trapping, Alcohol   More FDA Info for this Device
510(K) Number	K090766
Device Name	Devices, Breath Trapping, Alcohol
Applicant	LIFELOC TECHNOLOGIES, INC. 12441 W. 49TH AVE. SUITE 4 WHEAT RIDGE, CO 80033 US Other 510(k) Applications for this Company
Contact	MARK LARY Other 510(k) Applications for this Contact
Regulation Number	862.3050   More FDA Info for this Regulation Number
Classification Product Code	DJZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/23/2009
Decision Date	07/23/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	TX - Clinical Toxicology
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review