Gary Giancarlo
Country not established
- Devices
- 1
What Gary Giancarlo makes
Gary Giancarlo manufactures the LOGO-NU-WAY, a medical device designed for securing and stabilizing intravenous lines, catheters, or other tubular devices to the skin or clothing.
The LOGO-NU-WAY is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The manufacturer operates from the United States.
Catalogue
Logo-Nu-Way Ref K800186
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gary Giancarlo have in the registry?
The registry currently lists 1 device for Gary Giancarlo. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gary Giancarlo's devices?
Among its 1 most recently registered device, Gary Giancarlo has devices listed in FDA 510(k) (1 device).
What risk classes do Gary Giancarlo's devices fall under?
Among its 1 most recently registered device, the classes recorded for Gary Giancarlo's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gary Giancarlo in the registry?
The most recently registered devices listed for Gary Giancarlo include LOGO-NU-WAY.