FDA 510(k) Application Details - K070172

Device Classification Name	Dna-Reagents, Neisseria   More FDA Info for this Device
510(K) Number	K070172
Device Name	Dna-Reagents, Neisseria
Applicant	ROCHE DIAGNOSTICS CORPORATION 9115 HAGUE ROAD INDIANAPOLIS, IN 46256 US Other 510(k) Applications for this Company
Contact	THERESA AMBROSE BUSH Other 510(k) Applications for this Contact
Regulation Number	866.3390   More FDA Info for this Regulation Number
Classification Product Code	LSL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/18/2007
Decision Date	04/17/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	MI - Microbiology
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review