Cormed, Inc., Sub. C.R.Bard, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cormed, Inc., Sub. C.R.Bard, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Cormed, Inc., Sub. C.R.Bard, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1983 to 1986. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Cormed, Inc., Sub. C.R.Bard, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cormed, Inc., Sub. C.R.Bard, Inc.
8 devices
Cleared
Dec 18, 1986
BUTTERFLY NON-CORING NEEDLE SET
General Hospital
93d
Cleared
Mar 31, 1986
PERCUTANEOUS INTRODUCER KIT
Cardiovascular
55d
Cleared
Nov 26, 1985
PORT-GARD
General Hospital
57d
Cleared
May 17, 1985
STERILE CORMED MEDIPORT
General Hospital
70d
Cleared
Apr 09, 1985
CORMED II AMBULATORY INFUSION PUMP
General Hospital
48d
Cleared
Sep 05, 1984
CORMED HUBER POINT NEEDLE
General & Plastic Surgery
30d
Cleared
Mar 30, 1984
VASCULAR ACCESS CATH. REPAIR KIT
General Hospital
137d
Cleared
Jan 05, 1983
CORCATH H & B VASCULAR ACCESS CATHETER
General Hospital
35d