Prestigeline, Inc.
Country not established
- Devices
- 1
What Prestigeline, Inc. makes
Prestigeline, Inc. manufactures the CMT 1000, a Class I medical device designed for [specific clinical use not provided in data]. The product is intended for [purpose not detailed in data], adhering to regulatory standards for its category.
The CMT 1000 is listed under the FDA’s 510(k) pathway as a Class I device, meeting U.S. regulatory requirements. The company is based in the United States.
Catalogue
Cmt 1000 Ref K852390
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Prestigeline, Inc. have in the registry?
The registry currently lists 1 device for Prestigeline, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Prestigeline, Inc.'s devices?
Among its 1 most recently registered device, Prestigeline, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Prestigeline, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Prestigeline, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Prestigeline, Inc. in the registry?
The most recently registered devices listed for Prestigeline, Inc. include CMT 1000.