Cook Vascular, Inc.
Cook Vascular, Inc. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2014, with 1 FDA device recall on record.
Top product codes for Cook Vascular, Inc.
FDA recalls by Cook Vascular, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Cook Vascular, Inc.
- K142301 — Evolution Mechanical Dilator Sheath Set, Evolution Shortie Mechanical Dilator Sheath Set, SteadySheath Evolution Tissue Stabilization Sheath, SteadySheath Evolution Shortie Tissue Stabilization Sheath
- K141148 — EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET, EVOLUTION SHORTIE RL CONTROLLED-ROTATION DILATOR SHEATH SET
- K110347 — DOPPLER MONITOR
- K083482 — COOK VASCULAR VITAL-JECT POWER INJECTABLE SAFETY INFUSION SET
- K081425 — COOK VASCULAR INC. VITAL-PORT VASCULAR ACCESS SYSTEM POWER INJECTABLE PORT
- K061000 — EVOLUTION MECHANICAL DILATOR SHEATH SET MODELS-LR-EVN-7.0, LR-EVN-9.0
- K032223 — COOK VASCULAR PERFECTA ELECTROSURGICAL DISSECTION SYSTEM ERGONOMIC INTERMITTENT ACTIVATION SWITCH
- K023937 — COOK VASCULAR SERPENTA CORONARY SINUS INTRODUCER SYSTEM
- K022649 — COOK-SWARTZ DOPPLER FLOW PROBE
- K010128 — COOK VASCULAR PEEL-AWAY HEMOSTASIS VALVE
- K002958 — SHAPEABLE DOPPLER FLOW PROBE
- K010055 — COOK VASCULAR ELECTROSURGICAL DISSECTION SHEATH
Data sourced from openFDA. This site is unofficial and independent of the FDA.