FDA 510(k) Application Details - K070691

Device Classification Name	Culture Media, Selective And Differential   More FDA Info for this Device
510(K) Number	K070691
Device Name	Culture Media, Selective And Differential
Applicant	BECTON, DICKINSON & CO. 7 LOVETON CIR. SPARKS, MD 21152-0999 US Other 510(k) Applications for this Company
Contact	DENNIS R MERTZ Other 510(k) Applications for this Contact
Regulation Number	866.2360   More FDA Info for this Regulation Number
Classification Product Code	JSI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/13/2007
Decision Date	11/20/2007
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