Touritu Engineering Co., Inc.
Country not established
- Devices
- 1
What Touritu Engineering Co., Inc. makes
Touritu Engineering Co., Inc. manufactures the MS-2000, a medical device designed for [specific application not provided in data]. The product is intended for [purpose not detailed in data], adhering to regulatory standards for its category.
The MS-2000 is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company operates from the United States, where its device is registered.
Catalogue
Ms-2000 Ref K961144
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Touritu Engineering Co., Inc. have in the registry?
The registry currently lists 1 device for Touritu Engineering Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Touritu Engineering Co., Inc.'s devices?
Among its 1 most recently registered device, Touritu Engineering Co., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Touritu Engineering Co., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Touritu Engineering Co., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Touritu Engineering Co., Inc. in the registry?
The most recently registered devices listed for Touritu Engineering Co., Inc. include MS-2000.