FDA 510(k) Application Details - K002786

Device Classification Name	Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days   More FDA Info for this Device
510(K) Number	K002786
Device Name	Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days
Applicant	SUNSCOPE INTL., INC. 20250 ACACIA ST., SUITE 115 NEWPORT BEACH, CA 92660 US Other 510(k) Applications for this Company
Contact	JORGE HAIDER Other 510(k) Applications for this Contact
Regulation Number	880.5200   More FDA Info for this Regulation Number
Classification Product Code	FOZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/07/2000
Decision Date	11/17/2000
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