Bard Peripheral Vacular, Inc.
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- Devices
- 1
What Bard Peripheral Vacular, Inc. makes
Bard Peripheral Vascular, Inc. manufactures the CROSSER CTO Recanalization Catheter, a device designed for recanalizing chronic total occlusions in peripheral arteries, facilitating blood flow restoration in blocked vessels.
The CROSSER CTO Recanalization Catheter is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
CROSSER CTO Recanalization Catheter Ref K161208
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bard Peripheral Vacular, Inc. have in the registry?
The registry currently lists 1 device for Bard Peripheral Vacular, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bard Peripheral Vacular, Inc.'s devices?
Among its 1 most recently registered device, Bard Peripheral Vacular, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bard Peripheral Vacular, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bard Peripheral Vacular, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bard Peripheral Vacular, Inc. in the registry?
The most recently registered devices listed for Bard Peripheral Vacular, Inc. include CROSSER CTO Recanalization Catheter.