Catheter Research C/O Burditt, Bowles & Radzius is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Catheter Research C/O Burditt, Bowles & Radzius - FDA 510(k) Cleared ...
8
Total
8
Cleared
0
Denied
Catheter Research C/O Burditt, Bowles & Radzius has 8 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 8 cleared submissions from 1987 to 1993. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Catheter Research C/O Burditt, Bowles & Radzius Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Catheter Research C/O Burditt, Bowles & Radzius
8 devices
Cleared
Jun 29, 1993
CRI CYNOSAR CATHETER
Cardiovascular
312d
Cleared
May 26, 1993
CRI ELECTRONIC CONTROL SYSTEM
Cardiovascular
282d
Cleared
Jan 10, 1992
CRI VESSEL OCCLUSIN SYSTEM/CRI OCCLUSION COIL
Cardiovascular
92d
Cleared
Mar 06, 1991
CRI CYNOSAR CATHETER
Cardiovascular
135d
Cleared
Dec 17, 1990
CRI STEERABLE CATHETER CONTROL SYSTEM
Cardiovascular
55d
Cleared
Sep 14, 1990
CRI CYNOSAR CATHETER
Cardiovascular
234d
Cleared
Jan 05, 1989
MICRO-GUIDE SYSTEM
Cardiovascular
83d
Cleared
Dec 03, 1987
MICRO-GUIDE
Cardiovascular
287d