FDA 510(k) Application Details - K964654

Device Classification Name	Needle, Hypodermic, Single Lumen   More FDA Info for this Device
510(K) Number	K964654
Device Name	Needle, Hypodermic, Single Lumen
Applicant	BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC 1 BECTON DRIVE, BLDG 2, MAIL CODE 226 FRANKLIN LAKES, NJ 07417 US Other 510(k) Applications for this Company
Contact	GREGORY W MORGAN 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	11/20/1996
Decision Date	04/02/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review