FDA 510(k) Application Details - K032425

Device Classification Name	Introducer, Syringe Needle   More FDA Info for this Device
510(K) Number	K032425
Device Name	Introducer, Syringe Needle
Applicant	BIOGEN 14 CAMBRIDGE CENTER CAMBRIDGE, MA 02142 US Other 510(k) Applications for this Company
Contact	Michael Poirier Other 510(k) Applications for this Contact
Regulation Number	880.6920   More FDA Info for this Regulation Number
Classification Product Code	KZH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/06/2003
Decision Date	11/05/2003
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