FDA 510(k) Application Details - K023955

Device Classification Name	Station, Pipetting And Diluting, For Clinical Use   More FDA Info for this Device
510(K) Number	K023955
Device Name	Station, Pipetting And Diluting, For Clinical Use
Applicant	BECTON, DICKINSON & CO. 7 LOVETON CIR. SPARKS, MD 21152-0999 US Other 510(k) Applications for this Company
Contact	COLLEN A KISTLER Other 510(k) Applications for this Contact
Regulation Number	862.2750   More FDA Info for this Regulation Number
Classification Product Code	JQW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/27/2002
Decision Date	06/24/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review