Coeur Laboratories, Inc.
Coeur Laboratories, Inc. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 1997.
Top product codes for Coeur Laboratories, Inc.
Recent clearances by Coeur Laboratories, Inc.
- K971712 — COEUR 130 ML ANGIOGRAPHIC SYRINGE
- K965214 — COEUR FRONT LOAD INJECTOR RETROFIT KIT (C859-0002)
- K960965 — FRONT LOAD INJECTOR TURRET MODEL 859-0001/200 ML FRONT LOAD SYRINGE MODEL 853-0211
- K890292 — PCA-10, 10CC DISP. ANGIOGRAPHY CONTROL SYRINGE
- K885138 — CAPILLARY TUBE, BLOOD COLLECTION
- K885202 — 16 LONG CATHETER W/ADAPTER, 14 FR AND 12 FR
- K881646 — UROLOGICAL CATHETER
- K874579 — COEUR CONTROL SYRINGE
- K873597 — TUBING, POLYETHYLENE
- K823920 — COEURLOCK STERILE DISPOS. ANGIOGRAPHIC
Data sourced from openFDA. This site is unofficial and independent of the FDA.