FDA 510(k) Application Details - K010890

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K010890
Device Name	Syringe, Piston
Applicant	BECTON DICKINSON AND CO. 1 BECTON DR. FRANKLIN LAKES, NJ 07417-1880 US Other 510(k) Applications for this Company
Contact	PETER ZURLO Other 510(k) Applications for this Contact
Regulation Number	880.5860   More FDA Info for this Regulation Number
Classification Product Code	FMF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/26/2001
Decision Date	04/19/2001
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