FDA 510(k) Application Details - K982346

Device Classification Name	Catheter, Biliary, Diagnostic   More FDA Info for this Device
510(K) Number	K982346
Device Name	Catheter, Biliary, Diagnostic
Applicant	ANGIODYNAMICS, INC. 603 QUEENSBURY AVE. QUEENSBURY, NY 12804 US Other 510(k) Applications for this Company
Contact	BRIAN KUNST Other 510(k) Applications for this Contact
Regulation Number	876.5010   More FDA Info for this Regulation Number
Classification Product Code	FGE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/06/1998
Decision Date	01/29/1999
Decision	SESU - SE - WITH LIMITATIONS
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review