Bard Access Systems, Inc. (Bard Has Joined BD)
United StatesFDA applicant, unverified
- Devices
- 2
What Bard Access Systems, Inc. (Bard Has Joined BD) makes
Bard Access Systems manufactures acute central venous catheters, including the BD Centro Vena (7 French dual-lumen) and standard acute central lines. These devices are designed for short-term vascular access in clinical settings, facilitating intravenous therapies, fluid administration, and monitoring.
The company’s products fall under FDA Class II regulation and are listed via 510(k) clearance. The portfolio is registered in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
BD Acute Central Line Ref K190855
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bard Access Systems, Inc. (Bard Has Joined Bd) have in the registry?
The registry currently lists 2 devices for Bard Access Systems, Inc. (Bard Has Joined Bd). Devices recorded under merged duplicate company entries are counted once.
Which registries list Bard Access Systems, Inc. (Bard Has Joined Bd)'s devices?
Among its 2 most recently registered devices, Bard Access Systems, Inc. (Bard Has Joined Bd) has devices listed in FDA 510(k) (2 devices).
What risk classes do Bard Access Systems, Inc. (Bard Has Joined Bd)'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Bard Access Systems, Inc. (Bard Has Joined Bd)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bard Access Systems, Inc. (Bard Has Joined Bd) in the registry?
The most recently registered devices listed for Bard Access Systems, Inc. (Bard Has Joined Bd) include BD Centro Vena Acute Central Line (7 French Dual Lumen) and BD Acute Central Line.