Daig Corp. - FDA 510(k) Cleared Devices
Recent clearances: ALLIANCE LEFT HEART DELIVERY SYSTEM INTRODUCER, MODEL #407509, ULTRA-FLEX HEMOSTASIS INTRODUCER. MODEL 406XXX, SPYGLASS 5 FR ANGIOGRAPHIC CATHETER
63
Total
63
Cleared
0
Denied
FDA 510(k) Regulatory Record - Daig Corp. Cardiovascular ✕
63 devices
Cleared
Nov 29, 2000
ALLIANCE LEFT HEART DELIVERY SYSTEM INTRODUCER, MODEL #407509
Cardiovascular
331d
Cleared
May 15, 2000
ULTRA-FLEX HEMOSTASIS INTRODUCER. MODEL 406XXX
Cardiovascular
144d
Cleared
Oct 19, 1998
SPYGLASS 5 FR ANGIOGRAPHIC CATHETER
Cardiovascular
110d
Cleared
Sep 16, 1998
FAST-CATH INTRA-CARDIAC INTRODUCER
Cardiovascular
86d
Cleared
May 21, 1998
FAST-CATH (TM) INTRA-CARDIAC INTRODUCER
Cardiovascular
225d
Cleared
May 14, 1997
FAST-CATH TRANSSEPTAL CATHETER INTRODUCER
Cardiovascular
201d
Cleared
Feb 21, 1997
SPYGLASS ANGIOGRAPHIC CATHETER
Cardiovascular
71d
Cleared
Oct 15, 1996
SPYGLASS ANGIOGRAPHIC CATHETER
Cardiovascular
89d
Cleared
Nov 28, 1995
DIAG FAST-CATH DUO & TRIO REMOVABLE HEMOSTASIS ADAPTERS W/SIDEPORTS & 3-WAY...
Cardiovascular
74d
Cleared
Mar 03, 1995
CONTROL
Cardiovascular
182d
Cleared
Dec 27, 1994
DAIG DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER
Cardiovascular
232d
Cleared
Nov 24, 1993
CATHETER INTRODUCER MODIFICATION
Cardiovascular
89d
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