FDA 510(k) Application Details - K980278

Device Classification Name	Catheter, Percutaneous   More FDA Info for this Device
510(K) Number	K980278
Device Name	Catheter, Percutaneous
Applicant	URESIL CORP. 5418 W. TOUHY AVE. SKOKIE, IL 60077 US Other 510(k) Applications for this Company
Contact	MATTHEW CURTIS Other 510(k) Applications for this Contact
Regulation Number	870.1250   More FDA Info for this Regulation Number
Classification Product Code	DQY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/26/1998
Decision Date	11/20/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review