Coeur, Inc.
Coeur, Inc. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2017.
Top product codes for Coeur, Inc.
Recent clearances by Coeur, Inc.
- K170431 — CT Syringe for Stellant Injectors (with & without Spikes, Prime Tubes, & Fill Tubes), CT Syringe Dual Pack for Stellant Injectors (with & without Spikes, Prime Tubes, & Fill Tubes), Single Fascia and Ram Tip, Dual Fascia and Ram Tip
- K161471 — MR Syringe Dual Pack for Solaris Injectors
- K150902 — 330psi Extension Y-Line with Dual Check Valve
- K142745 — 125mL CT Syringe
- K140469 — MR SYRINGE DUAL PACK
- K133600 — COEUR, INC. FRONTLOAD FOR OPTIVANTAGE POWER INJECTOR
- K120892 — DISPOSABLE 330PSI EXTENSION LINES
- K113498 — DISPOSABLE TORQUE DEVICE
- K113132 — DISPOSABLE HEMOSTATIC Y-CONNECTORS
- K090487 — DISPOSABLE ANGIOGRAPHIC SYRINGES FOR USE WITH NEMOTO ANGIOGRAPHIC POWER, MODEL SY-125, C855-5150
- K070798 — ADAPTERS FOR CT, ANGIOGRAPHIC, AND/OR MRI POWER INJECTORS
- K071196 — DISPOSABLE HIGH PRESSURE INJECTION LINES WITH AND WITHOUT ROTATING ADAPTERS
- K063114 — DISPOSABLE TRANSFER SETS WITH AND WITHOUT SWABBABLE VALVES AND/OR CHECK VALVES
- K051799 — DISPOSABLE CT/MR SYRINGES FOR NEMOTO INJECTORS
Data sourced from openFDA. This site is unofficial and independent of the FDA.