Impra, Inc. - FDA 510(k) Cleared Devices
29
Total
24
Cleared
0
Denied
Impra, Inc. has 24 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 24 cleared submissions from 1979 to 2001. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Impra, Inc. Filter by specialty or product code using the sidebar.
29 devices
Cleared
May 14, 2001
IMPRA CARBOFLO EPTFE VASCULAR GRAFTS
Cardiovascular
138d
Cleared
Mar 27, 2001
IMPRA CARBOFLO VASCULAR GRAFT, IMPRA CARBOFLO VASCULAR GRAFTS FOR A-V ACCESS
Cardiovascular
90d
Cleared
Apr 22, 1999
BI-DIRECTIONAL TUNNELER
Cardiovascular
24d
Cleared
Dec 15, 1998
DISTAFLO BYPASS GRAFT
Cardiovascular
50d
Cleared
Nov 24, 1998
DISTAFLO BYPASS GRAFT
Cardiovascular
22d
Cleared
Nov 19, 1998
IMPRA HIGH POROSITY GRAFT
Cardiovascular
78d
Cleared
May 07, 1998
VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT
Cardiovascular
44d
Cleared
May 07, 1998
VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT
Cardiovascular
44d
Cleared
Apr 15, 1997
IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT
Cardiovascular
15d
Cleared
Mar 20, 1997
IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT
Cardiovascular
105d
Cleared
Jan 02, 1997
IMPRA CARBOFLO EPTFE VASCULAR GRAFT
Cardiovascular
73d
Cleared
Oct 03, 1996
IMPRA CARBOFLO EPTFE VASCULAR GRAFT
Cardiovascular
90d