Coeur Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Coeur Laboratories, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Coeur Laboratories, Inc. has 10 FDA 510(k) cleared medical devices. Based in US.
Historical record: 10 cleared submissions from 1983 to 1997. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Coeur Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Coeur Laboratories, Inc.
10 devices
Cleared
Oct 08, 1997
COEUR 130 ML ANGIOGRAPHIC SYRINGE
Cardiovascular
152d
Cleared
Mar 28, 1997
COEUR FRONT LOAD INJECTOR RETROFIT KIT (C859-0002)
Cardiovascular
88d
Cleared
Sep 12, 1996
FRONT LOAD INJECTOR TURRET MODEL 859-0001/200 ML FRONT LOAD SYRINGE MODEL...
Cardiovascular
185d
Cleared
Jun 22, 1989
PCA-10, 10CC DISP. ANGIOGRAPHY CONTROL SYRINGE
Cardiovascular
154d
Cleared
Feb 07, 1989
CAPILLARY TUBE, BLOOD COLLECTION
Hematology
54d
Cleared
Jan 31, 1989
16 LONG CATHETER W/ADAPTER, 14 FR AND 12 FR
Gastroenterology & Urology
46d
Cleared
Jun 16, 1988
UROLOGICAL CATHETER
Gastroenterology & Urology
62d
Cleared
Jan 19, 1988
COEUR CONTROL SYRINGE
General Hospital
74d
Cleared
Nov 12, 1987
TUBING, POLYETHYLENE
Cardiovascular
69d
Cleared
Feb 18, 1983
COEURLOCK STERILE DISPOS. ANGIOGRAPHIC
Cardiovascular
52d