Mckinley Infuser
Country not established
- Devices
- 1
What Mckinley Infuser makes
McKinley Infuser produces intravenous infusion devices, including the ACCUFUSER and ACCUFUSER PLUS for controlled medication delivery, along with associated procedure and infusion kits designed for hospital use.
The company’s products are classified as Class II devices under FDA regulations and are authorised via the 510(k) pathway. They are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mckinley Infuser have in the registry?
The registry currently lists 1 device for Mckinley Infuser. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mckinley Infuser's devices?
Among its 1 most recently registered device, Mckinley Infuser has devices listed in FDA 510(k) (1 device).
What risk classes do Mckinley Infuser's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mckinley Infuser's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mckinley Infuser in the registry?
The most recently registered devices listed for Mckinley Infuser include ACCUFUSER, ACCUFUSER PLUS, STANDARD PROCEDURE KIT, ACCUFUSER INFUSION KIT.