Neobit Co., Ltd.
Country not established
- Devices
- 1
What Neobit Co., Ltd. makes
Neobit Co., Ltd. manufactures MEDIPACS, a line of Class II medical devices designed for diagnostic imaging and patient monitoring applications, including portable X-ray systems and associated imaging solutions.
The company’s portfolio is regulated under the FDA’s 510(k) clearance process for Class II devices and is listed in the FDA’s 510(k) database. Neobit Co., Ltd. is headquartered in the United States.
Catalogue
Medipacs Ref K040486
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neobit Co., Ltd. have in the registry?
The registry currently lists 1 device for Neobit Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neobit Co., Ltd.'s devices?
Among its 1 most recently registered device, Neobit Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Neobit Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neobit Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neobit Co., Ltd. in the registry?
The most recently registered devices listed for Neobit Co., Ltd. include MEDIPACS.