Medical Device Manufacturer · US , NC

Coeur Laboratories, Inc.

10 submissions · 10 cleared · Since 1983
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.

10 devices
1–10 of 10
COEUR 130 ML ANGIOGRAPHIC SYRINGE
K971712 · DXT Injector And Syringe, Angiographic · Cardiovascular
Oct 1997 152d
COEUR FRONT LOAD INJECTOR RETROFIT KIT (C859-0002)
K965214 · DTX Gas Control Unit, Cardiopulmonary Bypass · Cardiovascular
Mar 1997 88d
FRONT LOAD INJECTOR TURRET MODEL 859-0001/200 ML FRONT LOAD SYRINGE MODEL 853-0211
K960965 · DXT Injector And Syringe, Angiographic · Cardiovascular
Sep 1996 185d
PCA-10, 10CC DISP. ANGIOGRAPHY CONTROL SYRINGE
K890292 · DXT Injector And Syringe, Angiographic · Cardiovascular
Jun 1989 154d
CAPILLARY TUBE, BLOOD COLLECTION
K885138 · GIO Tube, Collection, Capillary Blood · Hematology
Feb 1989 54d
16 LONG CATHETER W/ADAPTER, 14 FR AND 12 FR
K885202 · KOD Catheter, Urological · Gastroenterology & Urology
Jan 1989 46d
UROLOGICAL CATHETER
K881646 · KOD Catheter, Urological · Gastroenterology & Urology
Jun 1988 62d
COEUR CONTROL SYRINGE
K874579 · FMF Syringe, Piston · General Hospital
Jan 1988 74d
TUBING, POLYETHYLENE
K873597 · DXT Injector And Syringe, Angiographic · Cardiovascular
Nov 1987 69d
COEURLOCK STERILE DISPOS. ANGIOGRAPHIC
K823920 · DXT Injector And Syringe, Angiographic · Cardiovascular
Feb 1983 52d
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