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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.
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