Guidant Cardiac and Vascular Surgery
Country not established
- Devices
- 7
What Guidant Cardiac and Vascular Surgery makes
Guidant Cardiac and Vascular Surgery manufactures angiographic catheters, balloon catheters, sheaths, sheath introducers, marker boards, and retriever devices for cardiac and vascular procedures.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Evt Angioscale Angiographic Catheter Ref K970469
Regimes: 510(k) Registry: 510(k)Ancure Lliac Balloon Catheter Ref K003495
Regimes: 510(k) Registry: 510(k)Ancure Sheath Model # 40315, 40320, 40325 Ref K003889
Regimes: 510(k) Registry: 510(k)Evt Expandable Sheath Ref K970470
Regimes: 510(k) Registry: 510(k)Evt Marker Board Ref K970608
Regimes: 510(k) Registry: 510(k)Endovance Dualpass Tear-Away Sheath Introducer Ref K002676
Regimes: 510(k) Registry: 510(k)Guidant Retriever Device Ref K001694
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Guidant Cardiac and Vascular Surgery have in the registry?
The registry currently lists 7 devices for Guidant Cardiac and Vascular Surgery. Devices recorded under merged duplicate company entries are counted once.
Which registries list Guidant Cardiac and Vascular Surgery's devices?
Among its 7 most recently registered devices, Guidant Cardiac and Vascular Surgery has devices listed in FDA 510(k) (7 devices).
What risk classes do Guidant Cardiac and Vascular Surgery's devices fall under?
Among its 7 most recently registered devices, the classes recorded for Guidant Cardiac and Vascular Surgery's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Guidant Cardiac and Vascular Surgery in the registry?
The most recently registered devices listed for Guidant Cardiac and Vascular Surgery include EVT ANGIOSCALE ANGIOGRAPHIC CATHETER, ANCURE LLIAC BALLOON CATHETER, ANCURE SHEATH MODEL # 40315, 40320, 40325 and EVT EXPANDABLE SHEATH.