FDA 510(k) Application Details - K020185

Device Classification Name	System, Test, Automated, Antimicrobial Susceptibility, Short Incubation   More FDA Info for this Device
510(K) Number	K020185
Device Name	System, Test, Automated, Antimicrobial Susceptibility, Short Incubation
Applicant	DADE BEHRING, INC. 2040 ENTERPRISE BLVD. WEST SACRAMENTO, CA 95691 US Other 510(k) Applications for this Company
Contact	MAUREEN MENDE Other 510(k) Applications for this Contact
Regulation Number	866.1645   More FDA Info for this Regulation Number
Classification Product Code	LON Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/18/2002
Decision Date	02/06/2002
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