Hitron Corp.
Country not established
- Devices
- 1
What Hitron Corp. makes
Hitron Corp. manufactures the OCTOPUS, a medical device designed for [specific application not detailed in data]. The product is categorized under Class I devices, indicating low-risk medical instruments.
The OCTOPUS is regulated under the FDA’s 510(k) pathway and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Octopus Ref K780414
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hitron Corp. have in the registry?
The registry currently lists 1 device for Hitron Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hitron Corp.'s devices?
Among its 1 most recently registered device, Hitron Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Hitron Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hitron Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Hitron Corp. in the registry?
The most recently registered devices listed for Hitron Corp. include OCTOPUS.