Daig Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Daig Corp. - FDA 510(k) Cleared Devices
63
Total
63
Cleared
0
Denied
Daig Corp. has 63 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 63 cleared submissions from 1977 to 2000.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Daig Corp.
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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