Blockade Medical
Country not established
- Devices
- 6
What Blockade Medical makes
Blockade Medical manufactures the Barricade Embolization Coil System, a device designed for vascular embolization procedures to occlude blood vessels. It is intended for use in interventional radiology and neurovascular applications, including the treatment of arteriovenous malformations and aneurysms.
The Barricade Embolization Coil System is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Barricade Embolization Coil System Ref K123338
Regimes: 510(k) Registry: 510(k)Barricade Embolization Coil System Ref K142513
Regimes: 510(k) Registry: 510(k)Barricade Embolization Coil System Ref K131475
Regimes: 510(k) Registry: 510(k)Barricade Embolization Coil System Ref K151760
Regimes: 510(k) Registry: 510(k)Barricade Embolization Coil System Ref K132482
Regimes: 510(k) Registry: 510(k)Barricade Embolization Coil System Ref K140104
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Blockade Medical have in the registry?
The registry currently lists 6 devices for Blockade Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Blockade Medical's devices?
Among its 6 most recently registered devices, Blockade Medical has devices listed in FDA 510(k) (6 devices).
What risk classes do Blockade Medical's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Blockade Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Blockade Medical in the registry?
The most recently registered devices listed for Blockade Medical include BARRICADE EMBOLIZATION COIL SYSTEM.