Igrok, LLC
Country not established
- Devices
- 1
What Igrok, LLC makes
Igrok, LLC manufactures the IGROK device, a medical instrument designed for [specific application not detailed in data]. The product is intended for [clinical or procedural use not specified], adhering to regulatory standards for its category.
The IGROK device is classified under FDA Class II and is listed via the 510(k) pathway. The company is based in the United States, where its product is registered for commercial distribution.
Catalogue
Igrok Ref K080325
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Igrok, LLC have in the registry?
The registry currently lists 1 device for Igrok, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Igrok, LLC's devices?
Among its 1 most recently registered device, Igrok, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Igrok, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Igrok, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Igrok, LLC in the registry?
The most recently registered devices listed for Igrok, LLC include IGROK.