FDA 510(k) Application Details - K020842

Device Classification Name	Susceptibility Test Discs, Antimicrobial   More FDA Info for this Device
510(K) Number	K020842
Device Name	Susceptibility Test Discs, Antimicrobial
Applicant	BECTON DICKINSON & CO. 7 LOVETON CIR. SPARKS, MD 21152-0999 US Other 510(k) Applications for this Company
Contact	MICHELLE BANDY Other 510(k) Applications for this Contact
Regulation Number	866.1620   More FDA Info for this Regulation Number
Classification Product Code	JTN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/15/2002
Decision Date	05/15/2002
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