Becton, Dickinson and Company (Bard Access Systems, Inc.)
Country not established
- Devices
- 1
What Becton, Dickinson and Company (Bard Access Systems, Inc.) makes
Becton, Dickinson and Company (Bard Access Systems, Inc.) manufactures the PowerGlide Pro™ Midline Catheter, a peripheral intravenous catheter designed for short- to medium-term venous access in adult patients.
The company’s products are regulated as Class II medical devices in the US and are listed under the FDA’s 510(k) clearance pathway. Bard Access Systems, Inc. is based in the United States.
Catalogue
PowerGlide Pro™ Midline Catheter Ref K240359
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Becton, Dickinson and Company (Bard Access Systems, Inc.) have in the registry?
The registry currently lists 1 device for Becton, Dickinson and Company (Bard Access Systems, Inc.). Devices recorded under merged duplicate company entries are counted once.
Which registries list Becton, Dickinson and Company (Bard Access Systems, Inc.)'s devices?
Among its 1 most recently registered device, Becton, Dickinson and Company (Bard Access Systems, Inc.) has devices listed in FDA 510(k) (1 device).
What risk classes do Becton, Dickinson and Company (Bard Access Systems, Inc.)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Becton, Dickinson and Company (Bard Access Systems, Inc.)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Becton, Dickinson and Company (Bard Access Systems, Inc.) in the registry?
The most recently registered devices listed for Becton, Dickinson and Company (Bard Access Systems, Inc.) include PowerGlide Pro™ Midline Catheter.