FDA 510(k) Application Details - K960705

Device Classification Name	Device, Neurovascular Embolization   More FDA Info for this Device
510(K) Number	K960705
Device Name	Device, Neurovascular Embolization
Applicant	TARGET THERAPEUTICS 47201 LAKEVIEW DR. FREEMONT, CA 94538-6530 US Other 510(k) Applications for this Company
Contact	ABHI ACHARYA 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	02/21/1996
Decision Date	05/21/1996
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