FDA 510(k) Applications Submitted by DAIG CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K982187 06/22/1998 FAST-CATH INTRA-CARDIAC INTRODUCER DAIG CORP.
K973840 10/08/1997 FAST-CATH (TM) INTRA-CARDIAC INTRODUCER DAIG CORP.
K962805 07/18/1996 SPYGLASS ANGIOGRAPHIC CATHETER DAIG CORP.
K964518 10/25/1996 FAST-CATH TRANSSEPTAL CATHETER INTRODUCER DAIG CORP.
K965249 12/12/1996 SPYGLASS ANGIOGRAPHIC CATHETER DAIG CORP.
K982299 07/01/1998 SPYGLASS 5 FR ANGIOGRAPHIC CATHETER DAIG CORP.
K000004 01/03/2000 ALLIANCE LEFT HEART DELIVERY SYSTEM INTRODUCER, MODEL #407509 DAIG CORP.
K994334 12/23/1999 ULTRA-FLEX HEMOSTASIS INTRODUCER. MODEL 406XXX DAIG CORP.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact