FDA 510(k) Application Details - K014123

Device Classification Name	Susceptibility Test Powders, Antimycobacterial   More FDA Info for this Device
510(K) Number	K014123
Device Name	Susceptibility Test Powders, Antimycobacterial
Applicant	BECTON, DICKINSON & CO. 7 LOVETON CIR. SPARKS, MD 21152-0999 US Other 510(k) Applications for this Company
Contact	JODY J HOFFMANN Other 510(k) Applications for this Contact
Regulation Number	866.1640   More FDA Info for this Regulation Number
Classification Product Code	MJA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/17/2001
Decision Date	04/19/2002
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