Guidant Corporation, Cardiac Surgery
Guidant Corporation, Cardiac Surgery holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2008.
Top product codes for Guidant Corporation, Cardiac Surgery
Recent clearances by Guidant Corporation, Cardiac Surgery
- K080169 — HEARTSTRING III PROXIMAL SEAL SYSTEM
- K041340 — GUIDANT MICROWAVE ABLATION SYSTEM
- K023630 — ESSEX ASPIRATION/IRRIGATION INSTRUMENT WITH POSITIONING GUIDE, MODEL SY-1400
- K024071 — GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEM
- K023629 — ESSEX DISSECTION CANNULA, MODEL SXD-1100, ESSEX DISSECTION TIP, MODEL SXD-1200
- K022718 — VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002
- K020701 — SYNCRUS INTERNAL CARDIOVERSION SYSTEM
- K020143 — VASOVIEW 5 HARVESTING CANNULA
Data sourced from openFDA. This site is unofficial and independent of the FDA.