FDA 510(k) Application Details - K024112

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K024112
Device Name	Syringe, Piston
Applicant	BECTON DICKINSON & CO. 1 BECTON DR. FRANKLIN LAKES, NJ 07417-1880 US Other 510(k) Applications for this Company
Contact	JOHN A SCHALAGO 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	12/13/2002
Decision Date	01/09/2003
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