FDA 510(k) Application Details - K123300

Device Classification Name	Needle, Hypodermic, Single Lumen   More FDA Info for this Device
510(K) Number	K123300
Device Name	Needle, Hypodermic, Single Lumen
Applicant	BECTON DICKINSON & CO. 1 BECTON DR. MC 372 FRANKLIN LAKES, NJ 07417-1880 US Other 510(k) Applications for this Company
Contact	PASQUALE AMATO Other 510(k) Applications for this Contact
Regulation Number	880.5570   More FDA Info for this Regulation Number
Classification Product Code	FMI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/23/2012
Decision Date	01/18/2013
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review