US Fusion, LLC. Dba Truecare Biomedix-USA
Country not established
- Devices
- 1
What US Fusion, LLC. Dba Truecare Biomedix-USA makes
Us Fusion, LLC, doing business as Truecare Biomedix-USA, manufactures the Q-FLO Closed Male Luer Connector, a medical device designed for secure fluid pathway connections in clinical settings.
This device is classified as Class II by the U.S. Food and Drug Administration and is listed in the FDA 510(k) premarket notification database; the company is based in the United States.
Catalogue
Q-Flo Closed Male Luer Connector Ref K121554
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Us Fusion, LLC. Dba Truecare Biomedix-USA have in the registry?
The registry currently lists 1 device for Us Fusion, LLC. Dba Truecare Biomedix-USA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Us Fusion, LLC. Dba Truecare Biomedix-USA's devices?
Among its 1 most recently registered device, Us Fusion, LLC. Dba Truecare Biomedix-USA has devices listed in FDA 510(k) (1 device).
What risk classes do Us Fusion, LLC. Dba Truecare Biomedix-USA's devices fall under?
Among its 1 most recently registered device, the classes recorded for Us Fusion, LLC. Dba Truecare Biomedix-USA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Us Fusion, LLC. Dba Truecare Biomedix-USA in the registry?
The most recently registered devices listed for Us Fusion, LLC. Dba Truecare Biomedix-USA include Q-FLO CLOSED MALE LUER CONNECTOR.