Intervascular, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intervascular, Inc. - FDA 510(k) Cleared Devices
16
Total
13
Cleared
0
Denied
Intervascular, Inc. has 13 FDA 510(k) cleared cardiovascular devices. Based in Walker, US.
Historical record: 13 cleared submissions from 1984 to 2001.
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 - Intervascular, Inc.
16 devices
Cleared
Jan 08, 2001
INTERGARD KNITTED ULTRA THIN AND INTERGARD KNITTED COLLAGEN COATED AND...
Cardiovascular
670d
Cleared
Feb 22, 1999
MODIFICATION OF INTERGARD WOVEN COLLAGEN COATED VASCULAR PROSTHESES
Cardiovascular
83d
Cleared
Nov 24, 1998
INTERGARD KNITTED ULTRA THIN COLLAGEN COATED VASCULAR GRAFT AND HEMACAROTID...
Cardiovascular
26d
Cleared
Jun 05, 1997
INTERGARD WOVEN COLLAGEN COATED VASCULAR PROSTHESES
Cardiovascular
90d
Cleared
May 05, 1997
HEMAPATCH VASCULAR PATCHES, INTERGARD AND INTERGARD-RS VASCULAR PROSTHESES
Cardiovascular
171d
Cleared
Nov 25, 1992
ULTRA LOW POROSITY DACRON WOVEN PATCH
Cardiovascular
232d
Cleared
Oct 23, 1991
OCHSNER ULP BIFURCATION VASCULAR PROTHESIS
Cardiovascular
99d
Cleared
Sep 23, 1991
LOW POROSITY (LP) VASCULAR PROSTHESIS
Cardiovascular
83d
Cleared
Apr 02, 1991
OCHSNER 500 VASCULAR PROSTHESIS
Cardiovascular
130d
Cleared
Feb 15, 1991
OCHSNER 50 VASCULAR PROSTHESIS
Cardiovascular
84d
Cleared
Dec 03, 1990
OCHSNER 50 BIFURCATION
Cardiovascular
97d
Cleared
May 25, 1988
OCHSNER & MICRON FABRIC PATCH
Cardiovascular
44d