Sometec, Inc.
Country not established
- Devices
- 1
What Sometec, Inc. makes
Sometec, Inc. manufactures the DYNEMO 3000, a medical device designed for dynamic exercise testing and cardiac stress evaluation, used to assess cardiovascular function under controlled physical exertion.
The DYNEMO 3000 is classified as a Class II device under FDA regulations and is authorised via the 510(k) clearance process. The company is based in the United States.
Catalogue
Dynemo 3000 Ref K972798
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sometec, Inc. have in the registry?
The registry currently lists 1 device for Sometec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sometec, Inc.'s devices?
Among its 1 most recently registered device, Sometec, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sometec, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sometec, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sometec, Inc. in the registry?
The most recently registered devices listed for Sometec, Inc. include DYNEMO 3000.