FDA 510(k) Application Details - K964021

Device Classification Name	Device, Neurovascular Embolization   More FDA Info for this Device
510(K) Number	K964021
Device Name	Device, Neurovascular Embolization
Applicant	BAXTER EDWARDS 17221 RED HILL AVE. IRVINE, CA 92714-5686 US Other 510(k) Applications for this Company
Contact	PAULA A TORRIANNI Other 510(k) Applications for this Contact
Regulation Number	882.5950   More FDA Info for this Regulation Number
Classification Product Code	HCG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/07/1996
Decision Date	03/27/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review