Mckinley Medical, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Mckinley Medical, LLC makes
Mckinley Medical, LLC makes modifications to the Accufuser device and the Accufuser Plus Standard Procedure Kit, as well as the McKinley Saturation Catheter.
These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Mckinley Saturation Catheter Ref K060119
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mckinley Medical, LLC have in the registry?
The registry currently lists 2 devices for Mckinley Medical, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mckinley Medical, LLC's devices?
Among its 2 most recently registered devices, Mckinley Medical, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Mckinley Medical, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mckinley Medical, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mckinley Medical, LLC in the registry?
The most recently registered devices listed for Mckinley Medical, LLC include MODIFICATION TO ACCUFUSER, ACCUFUSER PLUS STANDARD PROCEDURE KIT and MCKINLEY SATURATION CATHETER.