FDA 510(k) Application Details - K083091

Device Classification Name	Device, Vascular, For Promoting Embolization   More FDA Info for this Device
510(K) Number	K083091
Device Name	Device, Vascular, For Promoting Embolization
Applicant	BIOCOMPATIBLES U.K. LIMITED 20310 SW 48TH STREET FT. LAUDERDALE, FL 33332 US Other 510(k) Applications for this Company
Contact	JOHN GREENBAUM Other 510(k) Applications for this Contact
Regulation Number	870.3300   More FDA Info for this Regulation Number
Classification Product Code	KRD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/17/2008
Decision Date	12/24/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review