Ives Egg Solutions
Country not established
- Devices
- 1
What Ives Egg Solutions makes
Ives Egg Solutions manufactures the Ives MR Conditional Cup Electrode, a specialized electrode designed for use in magnetic resonance (MR) imaging procedures. This device is intended to facilitate safe and accurate electrical signal transmission during MR-compatible applications, ensuring compatibility with magnetic resonance environments.
The Ives MR Conditional Cup Electrode is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Ives MR Conditional Cup Electrode Ref K171102
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ives Egg Solutions have in the registry?
The registry currently lists 1 device for Ives Egg Solutions. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ives Egg Solutions's devices?
Among its 1 most recently registered device, Ives Egg Solutions has devices listed in FDA 510(k) (1 device).
What risk classes do Ives Egg Solutions's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ives Egg Solutions's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ives Egg Solutions in the registry?
The most recently registered devices listed for Ives Egg Solutions include Ives MR Conditional Cup Electrode.