FDA 510(k) Application Details - K020523

Device Classification Name	More FDA Info for this Device
510(K) Number	K020523
Device Name	BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757
Applicant	BD ONE BECTON DRIVE MC226 FRANKLIN LAKES, NJ 07417 US Other 510(k) Applications for this Company
Contact	PASQUALE AMOTO Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	SCL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/19/2002
Decision Date	03/20/2002
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